ENST00000350026.11:c.3836A=
|
ENSP00000055163.8:p.Asp1279=
|
|
ENST00000414678.8:c.3905A=
|
ENSP00000412835.3:p.Asp1302=
|
|
ENST00000637015.2:c.4124A=
|
ENSP00000489729.2:p.Asp1375=
|
|
ENST00000346085.10:c.3875A=
|
ENSP00000344546.5:p.Asp1292=
|
|
ENST00000350026.10:c.3587A=
|
ENSP00000055163.7:p.Asp1196=
|
|
ENST00000414678.7:c.2153A=
|
ENSP00000412835.2:p.Asp718=
|
|
ENST00000635849.1:c.1316A=
|
ENSP00000490948.1:p.Asp439=
|
|
ENST00000635957.1:c.950A=
|
ENSP00000490385.1:p.Asp317=
|
|
ENST00000636930.2:c.3995A=
MANE Select
|
ENSP00000490491.2:p.Asp1332=
|
|
ENST00000636940.1:n.1992A=
|
|
|
ENST00000637015.1:c.1363A=
|
|
|
ENST00000637568.1:c.1277A=
|
|
|
ENST00000637741.1:n.661A=
|
|
|
ENST00000637810.1:c.1337A=
|
ENSP00000489636.1:p.Asp446=
|
|
ENST00000637904.1:c.1496A=
|
ENSP00000490550.1:p.Asp499=
|
|
ENST00000647938.1:c.3626A=
|
ENSP00000498155.1:p.Asp1209=
|
|
ENST00000346085.9:c.3626A=
|
ENSP00000344546.4:p.Asp1209=
|
|
ENST00000350026.9:c.3587A=
|
ENSP00000055163.7:p.Asp1196=
|
|
ENST00000414678.6:c.2153A=
|
ENSP00000412835.2:p.Asp718=
|
|
NM_017519.2:c.3587A=
|
NP_059989.2:p.Asp1196=
|
|
NM_020732.3:c.3626A=
|
NP_065783.3:p.Asp1209=
|
|
XM_005267069.3:c.3746A=
|
XP_005267126.2:p.Asp1249=
|
|
XM_011535984.1:c.2825A=
|
XP_011534286.1:p.Asp942=
|
|
XM_011535985.1:c.2645A=
|
XP_011534287.1:p.Asp882=
|
|
XM_011535986.1:c.2405A=
|
XP_011534288.1:p.Asp802=
|
|
XM_011535987.1:c.2024A=
|
XP_011534289.1:p.Asp675=
|
|
XM_011535988.1:c.887A=
|
XP_011534290.1:p.Asp296=
|
|
NM_001346813.1:c.3746A=
|
NP_001333742.1:p.Asp1249=
|
|
NM_001363725.1:c.1496A=
|
NP_001350654.1:p.Asp499=
|
|
XM_011535984.2:c.3956A=
|
XP_011534286.2:p.Asp1319=
|
|
XM_011535988.3:c.887A=
|
XP_011534290.1:p.Asp296=
|
|
XM_017011103.2:c.3857A=
|
XP_016866592.1:p.Asp1286=
|
|
XM_017011104.1:c.3827A=
|
XP_016866593.1:p.Asp1276=
|
|
XM_017011105.2:c.3797A=
|
XP_016866594.1:p.Asp1266=
|
|
XM_017011106.2:c.3668A=
|
XP_016866595.1:p.Asp1223=
|
|
XM_017011107.2:c.3647A=
|
XP_016866596.1:p.Asp1216=
|
|
XR_002956289.1:n.4039A=
|
|
|
NM_001363725.2:c.1496A=
|
NP_001350654.1:p.Asp499=
|
|
NM_001371656.1:c.3875A=
|
NP_001358585.1:p.Asp1292=
|
|
NM_001374820.1:c.3875A=
|
NP_001361749.1:p.Asp1292=
|
|
NM_001374828.1:c.3995A=
MANE Select
|
NP_001361757.1:p.Asp1332=
|
|
NM_017519.3:c.3836A=
|
NP_059989.3:p.Asp1279=
|
|