ENST00000456935.7:c.1113A>G
MANE Select
|
ENSP00000395473.2:p.Ser371=
|
|
ENST00000221363.8:c.1110A>G
|
ENSP00000221363.4:p.Ser370=
|
|
ENST00000456935.6:c.1113A>G
|
ENSP00000395473.2:p.Ser371=
|
|
ENST00000465830.1:n.277A>G
|
|
|
ENST00000466794.5:n.1012A>G
|
|
|
ENST00000495617.1:n.280+390A>G
|
|
|
NM_000528.3:c.1113A>G
|
NP_000519.2:p.Ser371=
|
|
NM_001173498.1:c.1110A>G
|
NP_001166969.1:p.Ser370=
|
|
XM_005259913.1:c.1116A>G
|
XP_005259970.1:p.Ser372=
|
|
XM_011528017.1:c.12A>G
|
XP_011526319.1:p.Ser4=
|
|
XM_005259913.2:c.1116A>G
|
XP_005259970.1:p.Ser372=
|
|
XM_024451518.1:c.12A>G
|
XP_024307286.1:p.Ser4=
|
|
NM_000528.4:c.1113A>G
MANE Select
|
NP_000519.2:p.Ser371=
|
|
NM_001173498.2:c.1110A>G
|
NP_001166969.1:p.Ser370=
|
|