ENST00000456935.7:c.1492A>G
MANE Select
|
ENSP00000395473.2:p.Ile498Val
|
|
ENST00000221363.8:c.1489A>G
|
ENSP00000221363.4:p.Ile497Val
|
|
ENST00000433513.5:n.98A>G
|
|
|
ENST00000456935.6:c.1492A>G
|
ENSP00000395473.2:p.Ile498Val
|
|
ENST00000466794.5:n.1391A>G
|
|
|
ENST00000495617.1:n.668A>G
|
|
|
ENST00000593686.1:c.102A>G
|
|
|
ENST00000595880.5:n.89A>G
|
|
|
NM_000528.3:c.1492A>G
|
NP_000519.2:p.Ile498Val
|
|
NM_001173498.1:c.1489A>G
|
NP_001166969.1:p.Ile497Val
|
|
XM_005259913.1:c.1495A>G
|
XP_005259970.1:p.Ile499Val
|
|
XM_011528017.1:c.391A>G
|
XP_011526319.1:p.Ile131Val
|
|
XM_005259913.2:c.1495A>G
|
XP_005259970.1:p.Ile499Val
|
|
XM_024451518.1:c.391A>G
|
XP_024307286.1:p.Ile131Val
|
|
NM_000528.4:c.1492A>G
MANE Select
|
NP_000519.2:p.Ile498Val
|
|
NM_001173498.2:c.1489A>G
|
NP_001166969.1:p.Ile497Val
|
|