ENST00000381129.8:c.1047G>T
MANE Select
|
ENSP00000370521.3:p.Glu349Asp
|
|
ENST00000250087.9:c.858G>T
|
ENSP00000250087.5:p.Glu286Asp
|
|
ENST00000381128.2:c.*919G>T
|
ENSP00000370520.2:n.*919G>T
|
|
ENST00000381129.7:c.1047G>T
|
ENSP00000370521.3:p.Glu349Asp
|
|
ENST00000570466.5:c.981G>T
|
ENSP00000461287.1:p.Glu327Asp
|
|
ENST00000570584.5:c.251+8351G>T
|
|
|
ENST00000574506.5:c.1011G>T
|
ENSP00000458456.1:p.Glu337Asp
|
|
ENST00000575265.5:c.*1018G>T
|
ENSP00000459673.1:n.*1018G>T
|
|
ENST00000576307.5:c.867G>T
|
ENSP00000459522.1:p.Glu289Asp
|
|
ENST00000576776.5:c.975G>T
|
ENSP00000460827.1:p.Glu325Asp
|
|
ENST00000621374.4:c.*65G>T
|
ENSP00000481337.1:n.*65G>T
|
|
NM_001033054.2:c.858G>T
|
NP_001028226.1:p.Glu286Asp
|
|
NM_001033055.2:c.867G>T
|
NP_001028227.1:p.Glu289Asp
|
|
NM_001285399.2:c.1011G>T
|
NP_001272328.1:p.Glu337Asp
|
|
NM_001285400.2:c.981G>T
|
NP_001272329.1:p.Glu327Asp
|
|
NM_001285401.2:c.975G>T
|
NP_001272330.1:p.Glu325Asp
|
|
NM_001285402.1:c.930G>T
|
NP_001272331.1:p.Glu310Asp
|
|
NM_014336.4:c.1047G>T
|
NP_055151.3:p.Glu349Asp
|
|
NM_001033054.3:c.858G>T
|
NP_001028226.1:p.Glu286Asp
|
|
NM_001033055.3:c.867G>T
|
NP_001028227.1:p.Glu289Asp
|
|
NM_001285399.3:c.1011G>T
|
NP_001272328.1:p.Glu337Asp
|
|
NM_001285400.3:c.981G>T
|
NP_001272329.1:p.Glu327Asp
|
|
NM_001285401.3:c.975G>T
|
NP_001272330.1:p.Glu325Asp
|
|
NM_001285402.2:c.930G>T
|
NP_001272331.1:p.Glu310Asp
|
|
NM_001285403.3:c.*1018G>T
|
NP_001272332.1:n.*1018G>T
|
|
NM_014336.5:c.1047G>T
MANE Select
|
NP_055151.3:p.Glu349Asp
|
|
NM_001285403.4:c.*1018G>T
|
NP_001272332.1:n.*1018G>T
|
|