ENST00000264380.9:c.3415G>A
MANE Select
|
ENSP00000264380.4:p.Ala1139Thr
|
|
ENST00000264380.8:c.3415G>A
|
ENSP00000264380.4:p.Ala1139Thr
|
|
ENST00000452564.1:c.3247G>A
|
ENSP00000405736.1:p.Ala1083Thr
|
|
NM_015040.3:c.3415G>A
|
NP_055855.2:p.Ala1139Thr
|
|
XM_011510778.1:c.3451G>A
|
XP_011509080.1:p.Ala1151Thr
|
|
XM_011510779.1:c.3451G>A
|
XP_011509081.1:p.Ala1151Thr
|
|
XM_011510780.1:c.3448G>A
|
XP_011509082.1:p.Ala1150Thr
|
|
XM_011510781.1:c.3433G>A
|
XP_011509083.1:p.Ala1145Thr
|
|
XM_011510782.1:c.3451G>A
|
XP_011509084.1:p.Ala1151Thr
|
|
XM_011510783.1:c.3283G>A
|
XP_011509085.1:p.Ala1095Thr
|
|
XM_011510784.1:c.3280G>A
|
XP_011509086.1:p.Ala1094Thr
|
|
XM_011510785.1:c.3265G>A
|
XP_011509087.1:p.Ala1089Thr
|
|
XM_011510786.1:c.3160G>A
|
XP_011509088.1:p.Ala1054Thr
|
|
XM_011510787.1:c.3157G>A
|
XP_011509089.1:p.Ala1053Thr
|
|
XM_011510788.1:c.3124G>A
|
XP_011509090.1:p.Ala1042Thr
|
|
XM_011510789.1:c.2974G>A
|
XP_011509091.1:p.Ala992Thr
|
|
XM_011510790.1:c.2458G>A
|
XP_011509092.1:p.Ala820Thr
|
|
XM_011510791.1:c.2458G>A
|
XP_011509093.1:p.Ala820Thr
|
|
XM_011510792.1:c.3451G>A
|
XP_011509094.1:p.Ala1151Thr
|
|
XR_922888.1:n.3588G>A
|
|
|
XM_011510778.3:c.3451G>A
|
XP_011509080.1:p.Ala1151Thr
|
|
XM_011510779.2:c.3451G>A
|
XP_011509081.1:p.Ala1151Thr
|
|
XM_011510780.2:c.3448G>A
|
XP_011509082.1:p.Ala1150Thr
|
|
XM_011510781.3:c.3433G>A
|
XP_011509083.1:p.Ala1145Thr
|
|
XM_011510782.3:c.3451G>A
|
XP_011509084.1:p.Ala1151Thr
|
|
XM_011510783.3:c.3283G>A
|
XP_011509085.1:p.Ala1095Thr
|
|
XM_011510784.2:c.3280G>A
|
XP_011509086.1:p.Ala1094Thr
|
|
XM_011510785.3:c.3265G>A
|
XP_011509087.1:p.Ala1089Thr
|
|
XM_011510786.3:c.3160G>A
|
XP_011509088.1:p.Ala1054Thr
|
|
XM_011510789.2:c.2974G>A
|
XP_011509091.1:p.Ala992Thr
|
|
XM_011510792.3:c.3451G>A
|
XP_011509094.1:p.Ala1151Thr
|
|
XM_017003568.1:c.3397G>A
|
XP_016859057.1:p.Ala1133Thr
|
|
XM_017003569.1:c.3229G>A
|
XP_016859058.1:p.Ala1077Thr
|
|
XM_017003570.1:c.2956G>A
|
XP_016859059.1:p.Ala986Thr
|
|
XM_017003571.1:c.2806G>A
|
XP_016859060.1:p.Ala936Thr
|
|
XM_017003572.1:c.2458G>A
|
XP_016859061.1:p.Ala820Thr
|
|
XM_017003573.1:c.2458G>A
|
XP_016859062.1:p.Ala820Thr
|
|
XM_017003574.1:c.2458G>A
|
XP_016859063.1:p.Ala820Thr
|
|
NM_015040.4:c.3415G>A
MANE Select
|
NP_055855.2:p.Ala1139Thr
|
|