ENST00000350026.11:c.3827T>C
|
ENSP00000055163.8:p.Val1276Ala
|
|
ENST00000414678.8:c.3896T>C
|
ENSP00000412835.3:p.Val1299Ala
|
|
ENST00000637015.2:c.4115T>C
|
ENSP00000489729.2:p.Val1372Ala
|
|
ENST00000346085.10:c.3866T>C
|
ENSP00000344546.5:p.Val1289Ala
|
|
ENST00000350026.10:c.3578T>C
|
ENSP00000055163.7:p.Val1193Ala
|
|
ENST00000414678.7:c.2144T>C
|
ENSP00000412835.2:p.Val715Ala
|
|
ENST00000635849.1:c.1307T>C
|
ENSP00000490948.1:p.Val436Ala
|
|
ENST00000635957.1:c.941T>C
|
ENSP00000490385.1:p.Val314Ala
|
|
ENST00000636930.2:c.3986T>C
MANE Select
|
ENSP00000490491.2:p.Val1329Ala
|
|
ENST00000636940.1:n.1983T>C
|
|
|
ENST00000637015.1:c.1354T>C
|
|
|
ENST00000637568.1:c.1268T>C
|
|
|
ENST00000637741.1:n.652T>C
|
|
|
ENST00000637810.1:c.1328T>C
|
ENSP00000489636.1:p.Val443Ala
|
|
ENST00000637904.1:c.1487T>C
|
ENSP00000490550.1:p.Val496Ala
|
|
ENST00000647938.1:c.3617T>C
|
ENSP00000498155.1:p.Val1206Ala
|
|
ENST00000346085.9:c.3617T>C
|
ENSP00000344546.4:p.Val1206Ala
|
|
ENST00000350026.9:c.3578T>C
|
ENSP00000055163.7:p.Val1193Ala
|
|
ENST00000414678.6:c.2144T>C
|
ENSP00000412835.2:p.Val715Ala
|
|
NM_017519.2:c.3578T>C
|
NP_059989.2:p.Val1193Ala
|
|
NM_020732.3:c.3617T>C
|
NP_065783.3:p.Val1206Ala
|
|
XM_005267069.3:c.3737T>C
|
XP_005267126.2:p.Val1246Ala
|
|
XM_011535984.1:c.2816T>C
|
XP_011534286.1:p.Val939Ala
|
|
XM_011535985.1:c.2636T>C
|
XP_011534287.1:p.Val879Ala
|
|
XM_011535986.1:c.2396T>C
|
XP_011534288.1:p.Val799Ala
|
|
XM_011535987.1:c.2015T>C
|
XP_011534289.1:p.Val672Ala
|
|
XM_011535988.1:c.878T>C
|
XP_011534290.1:p.Val293Ala
|
|
NM_001346813.1:c.3737T>C
|
NP_001333742.1:p.Val1246Ala
|
|
NM_001363725.1:c.1487T>C
|
NP_001350654.1:p.Val496Ala
|
|
XM_011535984.2:c.3947T>C
|
XP_011534286.2:p.Val1316Ala
|
|
XM_011535988.3:c.878T>C
|
XP_011534290.1:p.Val293Ala
|
|
XM_017011103.2:c.3848T>C
|
XP_016866592.1:p.Val1283Ala
|
|
XM_017011104.1:c.3818T>C
|
XP_016866593.1:p.Val1273Ala
|
|
XM_017011105.2:c.3788T>C
|
XP_016866594.1:p.Val1263Ala
|
|
XM_017011106.2:c.3659T>C
|
XP_016866595.1:p.Val1220Ala
|
|
XM_017011107.2:c.3638T>C
|
XP_016866596.1:p.Val1213Ala
|
|
XR_002956289.1:n.4030T>C
|
|
|
NM_001363725.2:c.1487T>C
|
NP_001350654.1:p.Val496Ala
|
|
NM_001371656.1:c.3866T>C
|
NP_001358585.1:p.Val1289Ala
|
|
NM_001374820.1:c.3866T>C
|
NP_001361749.1:p.Val1289Ala
|
|
NM_001374828.1:c.3986T>C
MANE Select
|
NP_001361757.1:p.Val1329Ala
|
|
NM_017519.3:c.3827T>C
|
NP_059989.3:p.Val1276Ala
|
|