ENST00000360319.9:c.7132+335G>T
|
ENSP00000353467.4:n.7132+335G>T
|
|
ENST00000369850.10:c.7156+335G>T
MANE Select
|
ENSP00000358866.3:n.7156+335G>T
|
|
ENST00000369856.8:c.7075+335G>T
|
ENSP00000358872.4:n.7075+335G>T
|
|
ENST00000422373.6:c.3937+335G>T
|
ENSP00000416926.2:n.3937+335G>T
|
|
ENST00000610817.5:c.7213+335G>T
|
ENSP00000480593.2:n.7213+335G>T
|
|
ENST00000673639.2:c.280-1884G>T
|
|
|
ENST00000676696.1:c.7435+335G>T
|
ENSP00000503392.1:n.7435+335G>T
|
|
ENST00000678304.1:n.2874+335G>T
|
|
|
ENST00000344736.8:c.7036+335G>T
|
ENSP00000358863.3:n.7036+335G>T
|
|
ENST00000360319.8:c.7132+335G>T
|
ENSP00000353467.4:n.7132+335G>T
|
|
ENST00000369850.7:c.7156+335G>T
|
ENSP00000358866.3:n.7156+335G>T
|
|
ENST00000369856.7:c.7075+335G>T
|
ENSP00000358872.4:n.7075+335G>T
|
|
ENST00000420627.5:c.7112+335G>T
|
ENSP00000408921.1:n.7112+335G>T
|
|
ENST00000422373.5:c.7132+335G>T
|
ENSP00000416926.1:n.7132+335G>T
|
|
ENST00000490936.5:n.4019G>T
|
|
|
ENST00000498411.1:n.68-1744G>T
|
|
|
ENST00000498491.5:n.197+335G>T
|
|
|
ENST00000610817.4:c.6160+335G>T
|
ENSP00000480593.1:n.6160+335G>T
|
|
NM_001110556.1:c.7156+335G>T
|
NP_001104026.1:n.7156+335G>T
|
|
NM_001456.3:c.7132+335G>T
|
NP_001447.2:n.7132+335G>T
|
|
XM_011531127.1:c.7060+335G>T
|
XP_011529429.1:n.7060+335G>T
|
|
XM_011531128.1:c.7036+335G>T
|
XP_011529430.1:n.7036+335G>T
|
|
XM_011531129.1:c.6982+335G>T
|
XP_011529431.1:n.6982+335G>T
|
|
XM_011531130.1:c.6958+335G>T
|
XP_011529432.1:n.6958+335G>T
|
|
XM_011531131.1:c.6955+335G>T
|
XP_011529433.1:n.6955+335G>T
|
|
NM_001110556.2:c.7156+335G>T
MANE Select
|
NP_001104026.1:n.7156+335G>T
|
|
NM_001456.4:c.7132+335G>T
|
NP_001447.2:n.7132+335G>T
|
|