ENST00000352480.10:c.818T>A
MANE Select
|
ENSP00000253004.6:p.Phe273Tyr
|
|
ENST00000352480.9:c.818T>A
|
ENSP00000253004.6:p.Phe273Tyr
|
|
ENST00000372386.6:n.89T>A
|
|
|
ENST00000372393.7:c.818T>A
|
ENSP00000361469.2:p.Phe273Tyr
|
|
ENST00000372394.5:c.818T>A
|
ENSP00000361471.1:p.Phe273Tyr
|
|
ENST00000470849.4:n.543T>A
|
|
|
ENST00000492400.5:n.327T>A
|
|
|
ENST00000493984.6:n.595T>A
|
|
|
NM_000050.4:c.818T>A
|
NP_000041.2:p.Phe273Tyr
|
|
NM_054012.3:c.818T>A
|
NP_446464.1:p.Phe273Tyr
|
|
XM_005272200.2:c.818T>A
|
XP_005272257.1:p.Phe273Tyr
|
|
XM_011518705.1:c.932T>A
|
XP_011517007.1:p.Phe311Tyr
|
|
XM_005272200.3:c.818T>A
|
XP_005272257.1:p.Phe273Tyr
|
|
XM_011518705.2:c.932T>A
|
XP_011517007.1:p.Phe311Tyr
|
|
XM_017014729.1:c.914T>A
|
XP_016870218.1:p.Phe305Tyr
|
|
NM_054012.4:c.818T>A
MANE Select
|
NP_446464.1:p.Phe273Tyr
|
|