ENST00000269980.7:c.971T>A
MANE Select
|
ENSP00000269980.2:p.Phe324Tyr
|
|
ENST00000269980.6:c.971T>A
|
ENSP00000269980.2:p.Phe324Tyr
|
|
ENST00000457836.6:c.905T>A
|
ENSP00000416000.2:p.Phe302Tyr
|
|
ENST00000535632.5:n.600T>A
|
|
|
ENST00000540732.3:c.1073T>A
|
ENSP00000443246.1:p.Phe358Tyr
|
|
ENST00000542943.5:c.884T>A
|
ENSP00000440345.1:p.Phe295Tyr
|
|
ENST00000595085.5:c.922+49T>A
|
ENSP00000471150.2:n.922+49T>A
|
|
NM_000709.3:c.971T>A
|
NP_000700.1:p.Phe324Tyr
|
|
NM_001164783.1:c.968T>A
|
NP_001158255.1:p.Phe323Tyr
|
|
NM_000709.4:c.971T>A
MANE Select
|
NP_000700.1:p.Phe324Tyr
|
|
NM_001164783.2:c.968T>A
|
NP_001158255.1:p.Phe323Tyr
|
|