ENST00000265724.8:c.3257T>A
|
ENSP00000265724.3:p.Phe1086Tyr
|
|
ENST00000622132.5:c.3257T>A
MANE Select
|
ENSP00000478255.1:p.Phe1086Tyr
|
|
ENST00000265724.7:c.3257T>A
|
ENSP00000265724.3:p.Phe1086Tyr
|
|
ENST00000475929.5:n.413T>A
|
|
|
ENST00000488737.6:n.899T>A
|
|
|
ENST00000496821.5:n.885T>A
|
|
|
ENST00000543898.5:c.3065T>A
|
ENSP00000444095.1:p.Phe1022Tyr
|
|
ENST00000622132.4:c.3257T>A
|
ENSP00000478255.1:p.Phe1086Tyr
|
|
NM_000927.4:c.3257T>A
|
NP_000918.2:p.Phe1086Tyr
|
|
NM_001348944.1:c.3257T>A
|
NP_001335873.1:p.Phe1086Tyr
|
|
NM_001348945.1:c.3467T>A
|
NP_001335874.1:p.Phe1156Tyr
|
|
NM_001348946.1:c.3257T>A
|
NP_001335875.1:p.Phe1086Tyr
|
|
NM_001348946.2:c.3257T>A
MANE Select
|
NP_001335875.1:p.Phe1086Tyr
|
|
NM_000927.5:c.3257T>A
|
NP_000918.2:p.Phe1086Tyr
|
|
NM_001348944.2:c.3257T>A
|
NP_001335873.1:p.Phe1086Tyr
|
|
NM_001348945.2:c.3467T>A
|
NP_001335874.1:p.Phe1156Tyr
|
|