ENST00000350026.11:c.4971C>G
|
ENSP00000055163.8:p.Val1657=
|
|
ENST00000414678.8:c.5040C>G
|
ENSP00000412835.3:p.Val1680=
|
|
ENST00000637015.2:c.5259C>G
|
ENSP00000489729.2:p.Val1753=
|
|
ENST00000346085.10:c.5010C>G
|
ENSP00000344546.5:p.Val1670=
|
|
ENST00000350026.10:c.4722C>G
|
ENSP00000055163.7:p.Val1574=
|
|
ENST00000414678.7:c.3288C>G
|
ENSP00000412835.2:p.Val1096=
|
|
ENST00000635849.1:c.2451C>G
|
ENSP00000490948.1:p.Val817=
|
|
ENST00000635957.1:c.2082C>G
|
ENSP00000490385.1:p.Val694=
|
|
ENST00000636227.1:n.3593C>G
|
|
|
ENST00000636254.1:n.1050C>G
|
|
|
ENST00000636930.2:c.5130C>G
MANE Select
|
ENSP00000490491.2:p.Val1710=
|
|
ENST00000636940.1:n.3127C>G
|
|
|
ENST00000637015.1:c.2498C>G
|
|
|
ENST00000637568.1:c.2412C>G
|
|
|
ENST00000637741.1:n.1796C>G
|
|
|
ENST00000637810.1:c.2472C>G
|
ENSP00000489636.1:p.Val824=
|
|
ENST00000637904.1:c.2631C>G
|
ENSP00000490550.1:p.Val877=
|
|
ENST00000647938.1:c.4761C>G
|
ENSP00000498155.1:p.Val1587=
|
|
ENST00000346085.9:c.4761C>G
|
ENSP00000344546.4:p.Val1587=
|
|
ENST00000350026.9:c.4722C>G
|
ENSP00000055163.7:p.Val1574=
|
|
ENST00000414678.6:c.3288C>G
|
ENSP00000412835.2:p.Val1096=
|
|
NM_017519.2:c.4722C>G
|
NP_059989.2:p.Val1574=
|
|
NM_020732.3:c.4761C>G
|
NP_065783.3:p.Val1587=
|
|
XM_005267069.3:c.4881C>G
|
XP_005267126.2:p.Val1627=
|
|
XM_011535984.1:c.3960C>G
|
XP_011534286.1:p.Val1320=
|
|
XM_011535985.1:c.3780C>G
|
XP_011534287.1:p.Val1260=
|
|
XM_011535986.1:c.3540C>G
|
XP_011534288.1:p.Val1180=
|
|
XM_011535987.1:c.3159C>G
|
XP_011534289.1:p.Val1053=
|
|
XM_011535988.1:c.2022C>G
|
XP_011534290.1:p.Val674=
|
|
NM_001346813.1:c.4881C>G
|
NP_001333742.1:p.Val1627=
|
|
NM_001363725.1:c.2631C>G
|
NP_001350654.1:p.Val877=
|
|
XM_011535984.2:c.5091C>G
|
XP_011534286.2:p.Val1697=
|
|
XM_011535988.3:c.2022C>G
|
XP_011534290.1:p.Val674=
|
|
XM_017011103.2:c.4992C>G
|
XP_016866592.1:p.Val1664=
|
|
XM_017011104.1:c.4962C>G
|
XP_016866593.1:p.Val1654=
|
|
XM_017011105.2:c.4932C>G
|
XP_016866594.1:p.Val1644=
|
|
XM_017011106.2:c.4803C>G
|
XP_016866595.1:p.Val1601=
|
|
XM_017011107.2:c.4782C>G
|
XP_016866596.1:p.Val1594=
|
|
XR_002956289.1:n.5077C>G
|
|
|
NM_001363725.2:c.2631C>G
|
NP_001350654.1:p.Val877=
|
|
NM_001371656.1:c.5010C>G
|
NP_001358585.1:p.Val1670=
|
|
NM_001374820.1:c.5010C>G
|
NP_001361749.1:p.Val1670=
|
|
NM_001374828.1:c.5130C>G
MANE Select
|
NP_001361757.1:p.Val1710=
|
|
NM_017519.3:c.4971C>G
|
NP_059989.3:p.Val1657=
|
|