ENST00000269980.7:c.352A>T
MANE Select
|
ENSP00000269980.2:p.Ile118Phe
|
|
ENST00000269980.6:c.352A>T
|
ENSP00000269980.2:p.Ile118Phe
|
|
ENST00000457836.6:c.286A>T
|
ENSP00000416000.2:p.Ile96Phe
|
|
ENST00000538423.5:n.478A>T
|
|
|
ENST00000540732.3:c.454A>T
|
ENSP00000443246.1:p.Ile152Phe
|
|
ENST00000541315.1:c.159A>T
|
|
|
ENST00000542943.5:c.288+170A>T
|
ENSP00000440345.1:n.288+170A>T
|
|
ENST00000595085.5:c.352A>T
|
ENSP00000471150.2:p.Ile118Phe
|
|
NM_000709.3:c.352A>T
|
NP_000700.1:p.Ile118Phe
|
|
NM_001164783.1:c.352A>T
|
NP_001158255.1:p.Ile118Phe
|
|
NM_000709.4:c.352A>T
MANE Select
|
NP_000700.1:p.Ile118Phe
|
|
NM_001164783.2:c.352A>T
|
NP_001158255.1:p.Ile118Phe
|
|