ENST00000525341.2:c.738G>A
|
|
|
ENST00000528641.7:c.572G>A
|
ENSP00000434982.3:p.Cys191Tyr
|
|
ENST00000529797.2:n.1273G>A
|
|
|
ENST00000682324.1:c.469-566G>A
|
ENSP00000508017.1:n.469-566G>A
|
|
ENST00000682659.1:c.392G>A
|
ENSP00000507351.1:p.Cys131Tyr
|
|
ENST00000682699.1:c.761G>A
|
ENSP00000507935.1:p.Cys254Tyr
|
|
ENST00000683237.1:c.761G>A
|
ENSP00000507343.1:p.Cys254Tyr
|
|
ENST00000683856.1:c.584G>A
|
ENSP00000507979.1:p.Cys195Tyr
|
|
ENST00000684006.1:c.761G>A
|
ENSP00000507269.1:p.Cys254Tyr
|
|
ENST00000684657.1:c.581G>A
|
ENSP00000507961.1:p.Cys194Tyr
|
|
ENST00000279146.8:c.761G>A
MANE Select
|
ENSP00000279146.3:p.Cys254Tyr
|
|
ENST00000279146.7:c.761G>A
|
ENSP00000279146.3:p.Cys254Tyr
|
|
ENST00000525341.1:c.413G>A
|
ENSP00000476993.1:p.Cys138Tyr
|
|
ENST00000528641.6:c.572G>A
|
ENSP00000434982.2:p.Cys191Tyr
|
|
NM_001302959.1:c.584G>A
|
NP_001289888.1:p.Cys195Tyr
|
|
NM_001302960.1:c.761G>A
|
NP_001289889.1:p.Cys254Tyr
|
|
NM_003977.3:c.761G>A
|
NP_003968.3:p.Cys254Tyr
|
|
XM_024448761.1:c.761G>A
|
XP_024304529.1:p.Cys254Tyr
|
|
NM_003977.4:c.761G>A
MANE Select
|
NP_003968.3:p.Cys254Tyr
|
|
NM_001302960.2:c.761G>A
|
NP_001289889.1:p.Cys254Tyr
|
|
NM_001302959.2:c.584G>A
|
NP_001289888.1:p.Cys195Tyr
|
|