ENST00000456935.7:c.1474T>A
MANE Select
|
ENSP00000395473.2:p.Phe492Ile
|
|
ENST00000221363.8:c.1471T>A
|
ENSP00000221363.4:p.Phe491Ile
|
|
ENST00000433513.5:n.80T>A
|
|
|
ENST00000456935.6:c.1474T>A
|
ENSP00000395473.2:p.Phe492Ile
|
|
ENST00000466794.5:n.1373T>A
|
|
|
ENST00000495617.1:n.650T>A
|
|
|
ENST00000593686.1:c.84T>A
|
|
|
ENST00000595880.5:n.71T>A
|
|
|
NM_000528.3:c.1474T>A
|
NP_000519.2:p.Phe492Ile
|
|
NM_001173498.1:c.1471T>A
|
NP_001166969.1:p.Phe491Ile
|
|
XM_005259913.1:c.1477T>A
|
XP_005259970.1:p.Phe493Ile
|
|
XM_011528017.1:c.373T>A
|
XP_011526319.1:p.Phe125Ile
|
|
XM_005259913.2:c.1477T>A
|
XP_005259970.1:p.Phe493Ile
|
|
XM_024451518.1:c.373T>A
|
XP_024307286.1:p.Phe125Ile
|
|
NM_000528.4:c.1474T>A
MANE Select
|
NP_000519.2:p.Phe492Ile
|
|
NM_001173498.2:c.1471T>A
|
NP_001166969.1:p.Phe491Ile
|
|