ENST00000438257.9:c.347A>T
MANE Select
|
ENSP00000405854.5:p.Asp116Val
|
|
ENST00000555750.2:c.*185A>T
|
ENSP00000450980.2:n.*185A>T
|
|
ENST00000422005.7:c.*148A>T
|
ENSP00000411438.4:n.*148A>T
|
|
ENST00000438257.8:c.347A>T
|
ENSP00000405854.4:p.Asp116Val
|
|
ENST00000555750.1:c.455A>T
|
ENSP00000450980.1:p.Asp152Val
|
|
ENST00000555844.1:c.431A>T
|
|
|
ENST00000556811.5:c.323A>T
|
|
|
ENST00000557010.5:c.347A>T
|
ENSP00000451419.1:p.Asp116Val
|
|
ENST00000557125.1:c.49-78A>T
|
ENSP00000450547.1:n.49-78A>T
|
|
NM_000793.5:c.347A>T
|
NP_000784.2:p.Asp116Val
|
|
NM_001007023.3:c.455A>T
|
NP_001007024.1:p.Asp152Val
|
|
NM_001242502.1:c.*148A>T
|
NP_001229431.1:n.*148A>T
|
|
NM_001242503.1:c.*148A>T
|
NP_001229432.1:n.*148A>T
|
|
NM_013989.4:c.347A>T
|
NP_054644.1:p.Asp116Val
|
|
NM_000793.6:c.347A>T
|
NP_000784.3:p.Asp116Val
|
|
NM_001324462.2:c.347A>T
|
NP_001311391.2:p.Asp116Val
|
|
NM_001366496.1:c.347A>T
|
NP_001353425.1:p.Asp116Val
|
|
NM_013989.5:c.347A>T
MANE Select
|
NP_054644.1:p.Asp116Val
|
|
NR_158990.1:n.487A>T
|
|
|
NR_158991.1:n.621A>T
|
|
|