ENST00000525341.2:c.568G>C
|
|
|
ENST00000528641.7:c.402G>C
|
ENSP00000434982.3:p.Glu134Asp
|
|
ENST00000529797.2:n.1103G>C
|
|
|
ENST00000682324.1:c.468+705G>C
|
ENSP00000508017.1:n.468+705G>C
|
|
ENST00000682659.1:c.222G>C
|
ENSP00000507351.1:p.Glu74Asp
|
|
ENST00000682699.1:c.591G>C
|
ENSP00000507935.1:p.Glu197Asp
|
|
ENST00000683237.1:c.591G>C
|
ENSP00000507343.1:p.Glu197Asp
|
|
ENST00000683856.1:c.414G>C
|
ENSP00000507979.1:p.Glu138Asp
|
|
ENST00000684006.1:c.591G>C
|
ENSP00000507269.1:p.Glu197Asp
|
|
ENST00000684657.1:c.411G>C
|
ENSP00000507961.1:p.Glu137Asp
|
|
ENST00000279146.8:c.591G>C
MANE Select
|
ENSP00000279146.3:p.Glu197Asp
|
|
ENST00000279146.7:c.591G>C
|
ENSP00000279146.3:p.Glu197Asp
|
|
ENST00000525341.1:c.243G>C
|
ENSP00000476993.1:p.Glu81Asp
|
|
ENST00000528641.6:c.402G>C
|
ENSP00000434982.2:p.Glu134Asp
|
|
NM_001302959.1:c.414G>C
|
NP_001289888.1:p.Glu138Asp
|
|
NM_001302960.1:c.591G>C
|
NP_001289889.1:p.Glu197Asp
|
|
NM_003977.3:c.591G>C
|
NP_003968.3:p.Glu197Asp
|
|
XM_024448761.1:c.591G>C
|
XP_024304529.1:p.Glu197Asp
|
|
NM_003977.4:c.591G>C
MANE Select
|
NP_003968.3:p.Glu197Asp
|
|
NM_001302960.2:c.591G>C
|
NP_001289889.1:p.Glu197Asp
|
|
NM_001302959.2:c.414G>C
|
NP_001289888.1:p.Glu138Asp
|
|