ENST00000269980.7:c.997A>T
MANE Select
|
ENSP00000269980.2:p.Ile333Phe
|
|
ENST00000269980.6:c.997A>T
|
ENSP00000269980.2:p.Ile333Phe
|
|
ENST00000457836.6:c.1006A>T
|
ENSP00000416000.2:p.Ile336Phe
|
|
ENST00000540732.3:c.1099A>T
|
ENSP00000443246.1:p.Ile367Phe
|
|
ENST00000542943.5:c.910A>T
|
ENSP00000440345.1:p.Ile304Phe
|
|
ENST00000595085.5:c.922+302A>T
|
ENSP00000471150.2:n.922+302A>T
|
|
NM_000709.3:c.997A>T
|
NP_000700.1:p.Ile333Phe
|
|
NM_001164783.1:c.994A>T
|
NP_001158255.1:p.Ile332Phe
|
|
NM_000709.4:c.997A>T
MANE Select
|
NP_000700.1:p.Ile333Phe
|
|
NM_001164783.2:c.994A>T
|
NP_001158255.1:p.Ile332Phe
|
|