ENST00000636937.2:c.1847A>T
|
ENSP00000516154.1:p.Glu616Val
|
|
ENST00000268124.11:c.1847A>T
MANE Select
|
ENSP00000268124.5:p.Glu616Val
|
|
ENST00000530292.3:c.1448A>T
|
ENSP00000432885.2:p.Glu483Val
|
|
ENST00000635986.2:c.1847A>T
|
ENSP00000490653.2:p.Glu616Val
|
|
ENST00000636774.1:c.*414A>T
|
ENSP00000489799.1:n.*414A>T
|
|
ENST00000637238.1:c.584A>T
|
ENSP00000490756.1:p.Glu195Val
|
|
ENST00000637264.1:c.919A>T
|
|
|
ENST00000666746.1:c.1424A>T
|
|
|
ENST00000670281.1:c.167A>T
|
ENSP00000499709.1:p.Glu56Val
|
|
ENST00000672071.1:n.2045A>T
|
|
|
ENST00000672923.2:n.1950A>T
|
|
|
ENST00000268124.9:c.1847A>T
|
ENSP00000268124.5:p.Glu616Val
|
|
ENST00000442287.6:c.1847A>T
|
ENSP00000399851.2:p.Glu616Val
|
|
ENST00000526314.2:c.229A>T
|
|
|
ENST00000526398.1:c.36A>T
|
|
|
ENST00000532584.5:n.49A>T
|
|
|
ENST00000631044.2:c.*1230A>T
|
ENSP00000486730.1:n.*1230A>T
|
|
NM_001126131.1:c.1847A>T
|
NP_001119603.1:p.Glu616Val
|
|
NM_002693.2:c.1847A>T
|
NP_002684.1:p.Glu616Val
|
|
NM_001126131.2:c.1847A>T
|
NP_001119603.1:p.Glu616Val
|
|
NM_002693.3:c.1847A>T
MANE Select
|
NP_002684.1:p.Glu616Val
|
|