ENST00000698881.1:c.1171T>G
|
ENSP00000514003.1:p.Ser391Ala
|
|
ENST00000418331.7:c.829T>G
MANE Select
|
ENSP00000400010.2:p.Ser277Ala
|
|
ENST00000418331.6:c.829T>G
|
ENSP00000400010.2:p.Ser277Ala
|
|
ENST00000440289.6:c.829T>G
|
ENSP00000409733.2:p.Ser277Ala
|
|
ENST00000613246.4:c.829T>G
|
ENSP00000477933.1:p.Ser277Ala
|
|
ENST00000615445.4:c.829T>G
|
ENSP00000479342.1:p.Ser277Ala
|
|
NM_001098503.1:c.829T>G
|
NP_001091973.1:p.Ser277Ala
|
|
NM_002843.3:c.829T>G
|
NP_002834.3:p.Ser277Ala
|
|
XM_011520249.1:c.862T>G
|
XP_011518551.1:p.Ser288Ala
|
|
XR_930883.1:n.1179T>G
|
|
|
XM_017018083.1:c.907T>G
|
XP_016873572.1:p.Ser303Ala
|
|
XM_017018084.1:c.850T>G
|
XP_016873573.1:p.Ser284Ala
|
|
XM_017018085.1:c.781T>G
|
XP_016873574.1:p.Ser261Ala
|
|
XR_930883.2:n.1238T>G
|
|
|
NM_002843.4:c.829T>G
MANE Select
|
NP_002834.3:p.Ser277Ala
|
|
NM_001098503.2:c.829T>G
|
NP_001091973.1:p.Ser277Ala
|
|