ENST00000350026.11:c.3906T>A
|
ENSP00000055163.8:p.Ser1302Arg
|
|
ENST00000414678.8:c.3975T>A
|
ENSP00000412835.3:p.Ser1325Arg
|
|
ENST00000637015.2:c.4194T>A
|
ENSP00000489729.2:p.Ser1398Arg
|
|
ENST00000346085.10:c.3945T>A
|
ENSP00000344546.5:p.Ser1315Arg
|
|
ENST00000350026.10:c.3657T>A
|
ENSP00000055163.7:p.Ser1219Arg
|
|
ENST00000414678.7:c.2223T>A
|
ENSP00000412835.2:p.Ser741Arg
|
|
ENST00000635849.1:c.1386T>A
|
ENSP00000490948.1:p.Ser462Arg
|
|
ENST00000635957.1:c.1017T>A
|
ENSP00000490385.1:p.Ser339Arg
|
|
ENST00000636930.2:c.4065T>A
MANE Select
|
ENSP00000490491.2:p.Ser1355Arg
|
|
ENST00000636940.1:n.2062T>A
|
|
|
ENST00000637015.1:c.1433T>A
|
|
|
ENST00000637568.1:c.1347T>A
|
|
|
ENST00000637741.1:n.731T>A
|
|
|
ENST00000637810.1:c.1407T>A
|
ENSP00000489636.1:p.Ser469Arg
|
|
ENST00000637904.1:c.1566T>A
|
ENSP00000490550.1:p.Ser522Arg
|
|
ENST00000647938.1:c.3696T>A
|
ENSP00000498155.1:p.Ser1232Arg
|
|
ENST00000346085.9:c.3696T>A
|
ENSP00000344546.4:p.Ser1232Arg
|
|
ENST00000350026.9:c.3657T>A
|
ENSP00000055163.7:p.Ser1219Arg
|
|
ENST00000414678.6:c.2223T>A
|
ENSP00000412835.2:p.Ser741Arg
|
|
NM_017519.2:c.3657T>A
|
NP_059989.2:p.Ser1219Arg
|
|
NM_020732.3:c.3696T>A
|
NP_065783.3:p.Ser1232Arg
|
|
XM_005267069.3:c.3816T>A
|
XP_005267126.2:p.Ser1272Arg
|
|
XM_011535984.1:c.2895T>A
|
XP_011534286.1:p.Ser965Arg
|
|
XM_011535985.1:c.2715T>A
|
XP_011534287.1:p.Ser905Arg
|
|
XM_011535986.1:c.2475T>A
|
XP_011534288.1:p.Ser825Arg
|
|
XM_011535987.1:c.2094T>A
|
XP_011534289.1:p.Ser698Arg
|
|
XM_011535988.1:c.957T>A
|
XP_011534290.1:p.Ser319Arg
|
|
NM_001346813.1:c.3816T>A
|
NP_001333742.1:p.Ser1272Arg
|
|
NM_001363725.1:c.1566T>A
|
NP_001350654.1:p.Ser522Arg
|
|
XM_011535984.2:c.4026T>A
|
XP_011534286.2:p.Ser1342Arg
|
|
XM_011535988.3:c.957T>A
|
XP_011534290.1:p.Ser319Arg
|
|
XM_017011103.2:c.3927T>A
|
XP_016866592.1:p.Ser1309Arg
|
|
XM_017011104.1:c.3897T>A
|
XP_016866593.1:p.Ser1299Arg
|
|
XM_017011105.2:c.3867T>A
|
XP_016866594.1:p.Ser1289Arg
|
|
XM_017011106.2:c.3738T>A
|
XP_016866595.1:p.Ser1246Arg
|
|
XM_017011107.2:c.3717T>A
|
XP_016866596.1:p.Ser1239Arg
|
|
XR_002956289.1:n.4109T>A
|
|
|
NM_001363725.2:c.1566T>A
|
NP_001350654.1:p.Ser522Arg
|
|
NM_001371656.1:c.3945T>A
|
NP_001358585.1:p.Ser1315Arg
|
|
NM_001374820.1:c.3945T>A
|
NP_001361749.1:p.Ser1315Arg
|
|
NM_001374828.1:c.4065T>A
MANE Select
|
NP_001361757.1:p.Ser1355Arg
|
|
NM_017519.3:c.3906T>A
|
NP_059989.3:p.Ser1302Arg
|
|