tenascin XB (TNXB) - 619 nt intron 28 reference sequence

(intronic numbering for coding DNA Reference Sequence)
         .         .         .         .         .         .  g.65165
gtgagtggggggacaggccctcgtccccaggtttacctctgcagcccccttgtgtttctc  c.9751+60

         .         .         .         .         .         .  g.65225
ctttggatcttggcacctcttttgactgggcctctaggtttctgtcttttctcccatgtt  c.9751+120

         .         .         .         .         .         .  g.65285
gctaatgatcctgcctcatccttggattcatggagactgtgtggagtcagatgggcaggt  c.9751+180

         .         .         .         .         .         .  g.65345
agtccatgccctgtttgttgtagcttccttctcccattgtgatctggaacctccatgttg  c.9751+240

         .         .         .         .         .         .  g.65405
ctcgtgtgctcatttgttagtcttcaggctcccttaaggagtattttagtggctcagaaa  c.9751+300

         .  g.65415
gtgcttcaga  c.9751+310

--------------------- middle of intron ---------------------
                                       g.65416                g.65424
                                       c.9752-309  tccagctgc  c.9752-301

.         .         .         .         .         .           g.65484
ccagatctgcatgtgccttcgaatgtagtgattgtgcgactttgcaggcgtttcctaacc  c.9752-241

.         .         .         .         .         .           g.65544
ttgtgcttcagattcctgcaaagttggggtgatgataataatggcacccacttcatatgt  c.9752-181

.         .         .         .         .         .           g.65604
tgtgcgagggttaaatgcaccactgtttgtgagctgcttacagcaatgcagggcacagat  c.9752-121

.         .         .         .         .         .           g.65664
tctaaaacaagcgttttagaggaggccgctaagaaatgctcactccagtcctgggagagc  c.9752-61

.         .         .         .         .         .           g.65724
actgcctcccttgcgcagggtcctgcctcctgacccatgggcctgctctgctcttttcag  c.9752-1