ENST00000392676.8:c.4271A>T
MANE Select
|
ENSP00000376443.2:p.Glu1424Val
|
|
ENST00000392676.7:c.4271A>T
|
ENSP00000376443.2:p.Glu1424Val
|
|
ENST00000586811.1:c.1169A>T
|
ENSP00000465351.1:p.Glu390Val
|
|
ENST00000586995.5:c.3333A>T
|
ENSP00000467251.1:n.3333A>T
|
|
ENST00000588877.5:c.4271A>T
|
ENSP00000467882.1:p.Glu1424Val
|
|
ENST00000591234.5:c.2213A>T
|
ENSP00000465766.1:n.2213A>T
|
|
NM_018672.4:c.4271A>T
|
NP_061142.2:p.Glu1424Val
|
|
NM_172232.3:c.4271A>T
|
NP_758424.1:p.Glu1424Val
|
|
NM_172232.4:c.4271A>T
MANE Select
|
NP_758424.1:p.Glu1424Val
|
|
NM_018672.5:c.4271A>T
|
NP_061142.2:p.Glu1424Val
|
|