ENST00000263038.9:c.790C>G
MANE Select
|
ENSP00000263038.4:p.His264Asp
|
|
ENST00000263038.8:c.790C>G
|
ENSP00000263038.4:p.His264Asp
|
|
ENST00000396913.6:c.490C>G
|
ENSP00000380121.2:p.His164Asp
|
|
ENST00000396920.7:c.739C>G
|
ENSP00000380126.3:p.His247Asp
|
|
ENST00000453759.6:c.490C>G
|
ENSP00000412525.2:p.His164Asp
|
|
NM_001037537.1:c.490C>G
|
NP_001032626.1:p.His164Asp
|
|
NM_006214.3:c.790C>G
|
NP_006205.1:p.His264Asp
|
|
XM_005252469.2:c.571C>G
|
XP_005252526.1:p.His191Asp
|
|
NM_001323080.1:c.490C>G
|
NP_001310009.1:p.His164Asp
|
|
NM_001323082.1:c.796C>G
|
NP_001310011.1:p.His266Asp
|
|
NM_001323083.1:c.526C>G
|
NP_001310012.1:p.His176Asp
|
|
NM_001323084.1:c.496C>G
|
NP_001310013.1:p.His166Asp
|
|
NM_006214.4:c.790C>G
MANE Select
|
NP_006205.1:p.His264Asp
|
|
NM_001037537.2:c.490C>G
|
NP_001032626.1:p.His164Asp
|
|
NM_001323080.2:c.490C>G
|
NP_001310009.1:p.His164Asp
|
|
NM_001323082.2:c.796C>G
|
NP_001310011.1:p.His266Asp
|
|
NM_001323083.2:c.526C>G
|
NP_001310012.1:p.His176Asp
|
|
NM_001323084.2:c.496C>G
|
NP_001310013.1:p.His166Asp
|
|