ENST00000350026.11:c.3936T>C
|
ENSP00000055163.8:p.Asp1312=
|
|
ENST00000414678.8:c.4005T>C
|
ENSP00000412835.3:p.Asp1335=
|
|
ENST00000637015.2:c.4224T>C
|
ENSP00000489729.2:p.Asp1408=
|
|
ENST00000346085.10:c.3975T>C
|
ENSP00000344546.5:p.Asp1325=
|
|
ENST00000350026.10:c.3687T>C
|
ENSP00000055163.7:p.Asp1229=
|
|
ENST00000414678.7:c.2253T>C
|
ENSP00000412835.2:p.Asp751=
|
|
ENST00000635849.1:c.1416T>C
|
ENSP00000490948.1:p.Asp472=
|
|
ENST00000635957.1:c.1047T>C
|
ENSP00000490385.1:p.Asp349=
|
|
ENST00000636930.2:c.4095T>C
MANE Select
|
ENSP00000490491.2:p.Asp1365=
|
|
ENST00000636940.1:n.2092T>C
|
|
|
ENST00000637015.1:c.1463T>C
|
|
|
ENST00000637568.1:c.1377T>C
|
|
|
ENST00000637741.1:n.761T>C
|
|
|
ENST00000637810.1:c.1437T>C
|
ENSP00000489636.1:p.Asp479=
|
|
ENST00000637904.1:c.1596T>C
|
ENSP00000490550.1:p.Asp532=
|
|
ENST00000647938.1:c.3726T>C
|
ENSP00000498155.1:p.Asp1242=
|
|
ENST00000346085.9:c.3726T>C
|
ENSP00000344546.4:p.Asp1242=
|
|
ENST00000350026.9:c.3687T>C
|
ENSP00000055163.7:p.Asp1229=
|
|
ENST00000414678.6:c.2253T>C
|
ENSP00000412835.2:p.Asp751=
|
|
NM_017519.2:c.3687T>C
|
NP_059989.2:p.Asp1229=
|
|
NM_020732.3:c.3726T>C
|
NP_065783.3:p.Asp1242=
|
|
XM_005267069.3:c.3846T>C
|
XP_005267126.2:p.Asp1282=
|
|
XM_011535984.1:c.2925T>C
|
XP_011534286.1:p.Asp975=
|
|
XM_011535985.1:c.2745T>C
|
XP_011534287.1:p.Asp915=
|
|
XM_011535986.1:c.2505T>C
|
XP_011534288.1:p.Asp835=
|
|
XM_011535987.1:c.2124T>C
|
XP_011534289.1:p.Asp708=
|
|
XM_011535988.1:c.987T>C
|
XP_011534290.1:p.Asp329=
|
|
NM_001346813.1:c.3846T>C
|
NP_001333742.1:p.Asp1282=
|
|
NM_001363725.1:c.1596T>C
|
NP_001350654.1:p.Asp532=
|
|
XM_011535984.2:c.4056T>C
|
XP_011534286.2:p.Asp1352=
|
|
XM_011535988.3:c.987T>C
|
XP_011534290.1:p.Asp329=
|
|
XM_017011103.2:c.3957T>C
|
XP_016866592.1:p.Asp1319=
|
|
XM_017011104.1:c.3927T>C
|
XP_016866593.1:p.Asp1309=
|
|
XM_017011105.2:c.3897T>C
|
XP_016866594.1:p.Asp1299=
|
|
XM_017011106.2:c.3768T>C
|
XP_016866595.1:p.Asp1256=
|
|
XM_017011107.2:c.3747T>C
|
XP_016866596.1:p.Asp1249=
|
|
XR_002956289.1:n.4139T>C
|
|
|
NM_001363725.2:c.1596T>C
|
NP_001350654.1:p.Asp532=
|
|
NM_001371656.1:c.3975T>C
|
NP_001358585.1:p.Asp1325=
|
|
NM_001374820.1:c.3975T>C
|
NP_001361749.1:p.Asp1325=
|
|
NM_001374828.1:c.4095T>C
MANE Select
|
NP_001361757.1:p.Asp1365=
|
|
NM_017519.3:c.3936T>C
|
NP_059989.3:p.Asp1312=
|
|