ENST00000269980.7:c.872A>T
MANE Select
|
ENSP00000269980.2:p.Tyr291Phe
|
|
ENST00000269980.6:c.872A>T
|
ENSP00000269980.2:p.Tyr291Phe
|
|
ENST00000457836.6:c.806A>T
|
ENSP00000416000.2:p.Tyr269Phe
|
|
ENST00000535632.5:n.501A>T
|
|
|
ENST00000540732.3:c.974A>T
|
ENSP00000443246.1:p.Tyr325Phe
|
|
ENST00000542943.5:c.785A>T
|
ENSP00000440345.1:p.Tyr262Phe
|
|
ENST00000545787.1:n.500A>T
|
|
|
ENST00000595085.5:c.872A>T
|
ENSP00000471150.2:p.Tyr291Phe
|
|
NM_000709.3:c.872A>T
|
NP_000700.1:p.Tyr291Phe
|
|
NM_001164783.1:c.869A>T
|
NP_001158255.1:p.Tyr290Phe
|
|
NM_000709.4:c.872A>T
MANE Select
|
NP_000700.1:p.Tyr291Phe
|
|
NM_001164783.2:c.869A>T
|
NP_001158255.1:p.Tyr290Phe
|
|