ENST00000525341.2:c.1109T>G
|
|
|
ENST00000528641.7:c.613T>G
|
ENSP00000434982.3:p.Tyr205Asp
|
|
ENST00000529797.2:n.1644T>G
|
|
|
ENST00000682324.1:c.469-195T>G
|
ENSP00000508017.1:n.469-195T>G
|
|
ENST00000682659.1:c.433T>G
|
ENSP00000507351.1:p.Tyr145Asp
|
|
ENST00000682699.1:c.802T>G
|
ENSP00000507935.1:p.Tyr268Asp
|
|
ENST00000683237.1:c.794T>G
|
ENSP00000507343.1:p.Leu265Arg
|
|
ENST00000683856.1:c.625T>G
|
ENSP00000507979.1:p.Tyr209Asp
|
|
ENST00000684006.1:c.791T>G
|
ENSP00000507269.1:p.Leu264Arg
|
|
ENST00000684657.1:c.622T>G
|
ENSP00000507961.1:p.Tyr208Asp
|
|
ENST00000279146.8:c.802T>G
MANE Select
|
ENSP00000279146.3:p.Tyr268Asp
|
|
ENST00000279146.7:c.802T>G
|
ENSP00000279146.3:p.Tyr268Asp
|
|
ENST00000528641.6:c.613T>G
|
ENSP00000434982.2:p.Tyr205Asp
|
|
NM_001302959.1:c.625T>G
|
NP_001289888.1:p.Tyr209Asp
|
|
NM_001302960.1:c.794T>G
|
NP_001289889.1:p.Leu265Arg
|
|
NM_003977.3:c.802T>G
|
NP_003968.3:p.Tyr268Asp
|
|
XM_024448761.1:c.802T>G
|
XP_024304529.1:p.Tyr268Asp
|
|
NM_003977.4:c.802T>G
MANE Select
|
NP_003968.3:p.Tyr268Asp
|
|
NM_001302960.2:c.794T>G
|
NP_001289889.1:p.Leu265Arg
|
|
NM_001302959.2:c.625T>G
|
NP_001289888.1:p.Tyr209Asp
|
|