ENST00000269980.7:c.354C>A
MANE Select
|
ENSP00000269980.2:p.Ile118=
|
|
ENST00000269980.6:c.354C>A
|
ENSP00000269980.2:p.Ile118=
|
|
ENST00000457836.6:c.288C>A
|
ENSP00000416000.2:p.Ile96=
|
|
ENST00000538423.5:n.480C>A
|
|
|
ENST00000540732.3:c.456C>A
|
ENSP00000443246.1:p.Ile152=
|
|
ENST00000541315.1:c.161C>A
|
|
|
ENST00000542943.5:c.288+172C>A
|
ENSP00000440345.1:n.288+172C>A
|
|
ENST00000595085.5:c.354C>A
|
ENSP00000471150.2:p.Ile118=
|
|
NM_000709.3:c.354C>A
|
NP_000700.1:p.Ile118=
|
|
NM_001164783.1:c.354C>A
|
NP_001158255.1:p.Ile118=
|
|
NM_000709.4:c.354C>A
MANE Select
|
NP_000700.1:p.Ile118=
|
|
NM_001164783.2:c.354C>A
|
NP_001158255.1:p.Ile118=
|
|