ENST00000263038.9:c.723A>T
MANE Select
|
ENSP00000263038.4:p.Glu241Asp
|
|
ENST00000263038.8:c.723A>T
|
ENSP00000263038.4:p.Glu241Asp
|
|
ENST00000396913.6:c.423A>T
|
ENSP00000380121.2:p.Glu141Asp
|
|
ENST00000396920.7:c.672A>T
|
ENSP00000380126.3:p.Glu224Asp
|
|
ENST00000453759.6:c.423A>T
|
ENSP00000412525.2:p.Glu141Asp
|
|
NM_001037537.1:c.423A>T
|
NP_001032626.1:p.Glu141Asp
|
|
NM_006214.3:c.723A>T
|
NP_006205.1:p.Glu241Asp
|
|
XM_005252469.2:c.504A>T
|
XP_005252526.1:p.Glu168Asp
|
|
NM_001323080.1:c.423A>T
|
NP_001310009.1:p.Glu141Asp
|
|
NM_001323082.1:c.729A>T
|
NP_001310011.1:p.Glu243Asp
|
|
NM_001323083.1:c.459A>T
|
NP_001310012.1:p.Glu153Asp
|
|
NM_001323084.1:c.429A>T
|
NP_001310013.1:p.Glu143Asp
|
|
NM_006214.4:c.723A>T
MANE Select
|
NP_006205.1:p.Glu241Asp
|
|
NM_001037537.2:c.423A>T
|
NP_001032626.1:p.Glu141Asp
|
|
NM_001323080.2:c.423A>T
|
NP_001310009.1:p.Glu141Asp
|
|
NM_001323082.2:c.729A>T
|
NP_001310011.1:p.Glu243Asp
|
|
NM_001323083.2:c.459A>T
|
NP_001310012.1:p.Glu153Asp
|
|
NM_001323084.2:c.429A>T
|
NP_001310013.1:p.Glu143Asp
|
|