ENST00000381129.8:c.1023G>C
MANE Select
|
ENSP00000370521.3:p.Glu341Asp
|
|
ENST00000250087.9:c.834G>C
|
ENSP00000250087.5:p.Glu278Asp
|
|
ENST00000381128.2:c.*895G>C
|
ENSP00000370520.2:n.*895G>C
|
|
ENST00000381129.7:c.1023G>C
|
ENSP00000370521.3:p.Glu341Asp
|
|
ENST00000570466.5:c.957G>C
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ENSP00000461287.1:p.Glu319Asp
|
|
ENST00000570584.5:c.251+8327G>C
|
|
|
ENST00000574506.5:c.987G>C
|
ENSP00000458456.1:p.Glu329Asp
|
|
ENST00000575265.5:c.*994G>C
|
ENSP00000459673.1:n.*994G>C
|
|
ENST00000576307.5:c.843G>C
|
ENSP00000459522.1:p.Glu281Asp
|
|
ENST00000576776.5:c.951G>C
|
ENSP00000460827.1:p.Glu317Asp
|
|
ENST00000621374.4:c.*41G>C
|
ENSP00000481337.1:n.*41G>C
|
|
NM_001033054.2:c.834G>C
|
NP_001028226.1:p.Glu278Asp
|
|
NM_001033055.2:c.843G>C
|
NP_001028227.1:p.Glu281Asp
|
|
NM_001285399.2:c.987G>C
|
NP_001272328.1:p.Glu329Asp
|
|
NM_001285400.2:c.957G>C
|
NP_001272329.1:p.Glu319Asp
|
|
NM_001285401.2:c.951G>C
|
NP_001272330.1:p.Glu317Asp
|
|
NM_001285402.1:c.906G>C
|
NP_001272331.1:p.Glu302Asp
|
|
NM_014336.4:c.1023G>C
|
NP_055151.3:p.Glu341Asp
|
|
NM_001033054.3:c.834G>C
|
NP_001028226.1:p.Glu278Asp
|
|
NM_001033055.3:c.843G>C
|
NP_001028227.1:p.Glu281Asp
|
|
NM_001285399.3:c.987G>C
|
NP_001272328.1:p.Glu329Asp
|
|
NM_001285400.3:c.957G>C
|
NP_001272329.1:p.Glu319Asp
|
|
NM_001285401.3:c.951G>C
|
NP_001272330.1:p.Glu317Asp
|
|
NM_001285402.2:c.906G>C
|
NP_001272331.1:p.Glu302Asp
|
|
NM_001285403.3:c.*994G>C
|
NP_001272332.1:n.*994G>C
|
|
NM_014336.5:c.1023G>C
MANE Select
|
NP_055151.3:p.Glu341Asp
|
|
NM_001285403.4:c.*994G>C
|
NP_001272332.1:n.*994G>C
|
|