ENST00000255266.10:c.1715T>A
MANE Select
|
ENSP00000255266.5:p.Phe572Tyr
|
|
ENST00000255266.9:c.1715T>A
|
ENSP00000255266.5:p.Phe572Tyr
|
|
ENST00000508173.5:n.1899T>A
|
|
|
ENST00000613228.1:c.1472T>A
|
ENSP00000478060.1:p.Phe491Tyr
|
|
ENST00000617647.4:c.1472T>A
|
ENSP00000482774.1:p.Phe491Tyr
|
|
NM_000440.2:c.1715T>A
|
NP_000431.2:p.Phe572Tyr
|
|
XM_011537648.1:c.1715T>A
|
XP_011535950.1:p.Phe572Tyr
|
|
XM_011537649.1:c.1169T>A
|
XP_011535951.1:p.Phe390Tyr
|
|
XM_011537650.1:c.830T>A
|
XP_011535952.1:p.Phe277Tyr
|
|
XM_011537651.1:c.668T>A
|
XP_011535953.1:p.Phe223Tyr
|
|
XM_011537652.1:c.638T>A
|
XP_011535954.1:p.Phe213Tyr
|
|
XM_011537653.1:c.638T>A
|
XP_011535955.1:p.Phe213Tyr
|
|
XM_011537654.1:c.638T>A
|
XP_011535956.1:p.Phe213Tyr
|
|
XM_011537650.2:c.830T>A
|
XP_011535952.1:p.Phe277Tyr
|
|
XM_011537651.2:c.668T>A
|
XP_011535953.1:p.Phe223Tyr
|
|
XM_011537653.2:c.638T>A
|
XP_011535955.1:p.Phe213Tyr
|
|
XM_011537654.2:c.638T>A
|
XP_011535956.1:p.Phe213Tyr
|
|
XM_017009572.2:c.1472T>A
|
XP_016865061.1:p.Phe491Tyr
|
|
NM_000440.3:c.1715T>A
MANE Select
|
NP_000431.2:p.Phe572Tyr
|
|