ENST00000269980.7:c.362A>T
MANE Select
|
ENSP00000269980.2:p.Glu121Val
|
|
ENST00000269980.6:c.362A>T
|
ENSP00000269980.2:p.Glu121Val
|
|
ENST00000457836.6:c.296A>T
|
ENSP00000416000.2:p.Glu99Val
|
|
ENST00000538423.5:n.488A>T
|
|
|
ENST00000540732.3:c.464A>T
|
ENSP00000443246.1:p.Glu155Val
|
|
ENST00000541315.1:c.169A>T
|
|
|
ENST00000542943.5:c.288+180A>T
|
ENSP00000440345.1:n.288+180A>T
|
|
ENST00000595085.5:c.362A>T
|
ENSP00000471150.2:p.Glu121Val
|
|
NM_000709.3:c.362A>T
|
NP_000700.1:p.Glu121Val
|
|
NM_001164783.1:c.362A>T
|
NP_001158255.1:p.Glu121Val
|
|
NM_000709.4:c.362A>T
MANE Select
|
NP_000700.1:p.Glu121Val
|
|
NM_001164783.2:c.362A>T
|
NP_001158255.1:p.Glu121Val
|
|