ENST00000350026.11:c.4484A>G
|
ENSP00000055163.8:p.Tyr1495Cys
|
|
ENST00000414678.8:c.4553A>G
|
ENSP00000412835.3:p.Tyr1518Cys
|
|
ENST00000637015.2:c.4772A>G
|
ENSP00000489729.2:p.Tyr1591Cys
|
|
ENST00000346085.10:c.4523A>G
|
ENSP00000344546.5:p.Tyr1508Cys
|
|
ENST00000350026.10:c.4235A>G
|
ENSP00000055163.7:p.Tyr1412Cys
|
|
ENST00000414678.7:c.2801A>G
|
ENSP00000412835.2:p.Tyr934Cys
|
|
ENST00000635849.1:c.1964A>G
|
ENSP00000490948.1:p.Tyr655Cys
|
|
ENST00000635957.1:c.1595A>G
|
ENSP00000490385.1:p.Tyr532Cys
|
|
ENST00000636227.1:n.3106A>G
|
|
|
ENST00000636254.1:n.563A>G
|
|
|
ENST00000636930.2:c.4643A>G
MANE Select
|
ENSP00000490491.2:p.Tyr1548Cys
|
|
ENST00000636940.1:n.2640A>G
|
|
|
ENST00000637015.1:c.2011A>G
|
|
|
ENST00000637568.1:c.1925A>G
|
|
|
ENST00000637741.1:n.1309A>G
|
|
|
ENST00000637810.1:c.1985A>G
|
ENSP00000489636.1:p.Tyr662Cys
|
|
ENST00000637904.1:c.2144A>G
|
ENSP00000490550.1:p.Tyr715Cys
|
|
ENST00000647938.1:c.4274A>G
|
ENSP00000498155.1:p.Tyr1425Cys
|
|
ENST00000346085.9:c.4274A>G
|
ENSP00000344546.4:p.Tyr1425Cys
|
|
ENST00000350026.9:c.4235A>G
|
ENSP00000055163.7:p.Tyr1412Cys
|
|
ENST00000414678.6:c.2801A>G
|
ENSP00000412835.2:p.Tyr934Cys
|
|
NM_017519.2:c.4235A>G
|
NP_059989.2:p.Tyr1412Cys
|
|
NM_020732.3:c.4274A>G
|
NP_065783.3:p.Tyr1425Cys
|
|
XM_005267069.3:c.4394A>G
|
XP_005267126.2:p.Tyr1465Cys
|
|
XM_011535984.1:c.3473A>G
|
XP_011534286.1:p.Tyr1158Cys
|
|
XM_011535985.1:c.3293A>G
|
XP_011534287.1:p.Tyr1098Cys
|
|
XM_011535986.1:c.3053A>G
|
XP_011534288.1:p.Tyr1018Cys
|
|
XM_011535987.1:c.2672A>G
|
XP_011534289.1:p.Tyr891Cys
|
|
XM_011535988.1:c.1535A>G
|
XP_011534290.1:p.Tyr512Cys
|
|
NM_001346813.1:c.4394A>G
|
NP_001333742.1:p.Tyr1465Cys
|
|
NM_001363725.1:c.2144A>G
|
NP_001350654.1:p.Tyr715Cys
|
|
XM_011535984.2:c.4604A>G
|
XP_011534286.2:p.Tyr1535Cys
|
|
XM_011535988.3:c.1535A>G
|
XP_011534290.1:p.Tyr512Cys
|
|
XM_017011103.2:c.4505A>G
|
XP_016866592.1:p.Tyr1502Cys
|
|
XM_017011104.1:c.4475A>G
|
XP_016866593.1:p.Tyr1492Cys
|
|
XM_017011105.2:c.4445A>G
|
XP_016866594.1:p.Tyr1482Cys
|
|
XM_017011106.2:c.4316A>G
|
XP_016866595.1:p.Tyr1439Cys
|
|
XM_017011107.2:c.4295A>G
|
XP_016866596.1:p.Tyr1432Cys
|
|
XR_002956289.1:n.4590A>G
|
|
|
NM_001363725.2:c.2144A>G
|
NP_001350654.1:p.Tyr715Cys
|
|
NM_001371656.1:c.4523A>G
|
NP_001358585.1:p.Tyr1508Cys
|
|
NM_001374820.1:c.4523A>G
|
NP_001361749.1:p.Tyr1508Cys
|
|
NM_001374828.1:c.4643A>G
MANE Select
|
NP_001361757.1:p.Tyr1548Cys
|
|
NM_017519.3:c.4484A>G
|
NP_059989.3:p.Tyr1495Cys
|
|