ENST00000636937.2:c.1584A>T
|
ENSP00000516154.1:p.Glu528Asp
|
|
ENST00000268124.11:c.1584A>T
MANE Select
|
ENSP00000268124.5:p.Glu528Asp
|
|
ENST00000530292.3:c.1185A>T
|
ENSP00000432885.2:p.Glu395Asp
|
|
ENST00000635986.2:c.1584A>T
|
ENSP00000490653.2:p.Glu528Asp
|
|
ENST00000636774.1:c.*151A>T
|
ENSP00000489799.1:n.*151A>T
|
|
ENST00000637238.1:c.321A>T
|
ENSP00000490756.1:p.Glu107Asp
|
|
ENST00000637264.1:c.656A>T
|
|
|
ENST00000666746.1:c.1161A>T
|
|
|
ENST00000672071.1:n.1782A>T
|
|
|
ENST00000672923.2:n.1687A>T
|
|
|
ENST00000268124.9:c.1584A>T
|
ENSP00000268124.5:p.Glu528Asp
|
|
ENST00000442287.6:c.1584A>T
|
ENSP00000399851.2:p.Glu528Asp
|
|
ENST00000631044.2:c.*967A>T
|
ENSP00000486730.1:n.*967A>T
|
|
NM_001126131.1:c.1584A>T
|
NP_001119603.1:p.Glu528Asp
|
|
NM_002693.2:c.1584A>T
|
NP_002684.1:p.Glu528Asp
|
|
NM_001126131.2:c.1584A>T
|
NP_001119603.1:p.Glu528Asp
|
|
NM_002693.3:c.1584A>T
MANE Select
|
NP_002684.1:p.Glu528Asp
|
|