ENST00000456935.7:c.1112C>G
MANE Select
|
ENSP00000395473.2:p.Ser371Ter
|
|
ENST00000221363.8:c.1109C>G
|
ENSP00000221363.4:p.Ser370Ter
|
|
ENST00000456935.6:c.1112C>G
|
ENSP00000395473.2:p.Ser371Ter
|
|
ENST00000465830.1:n.276C>G
|
|
|
ENST00000466794.5:n.1011C>G
|
|
|
ENST00000495617.1:n.280+389C>G
|
|
|
NM_000528.3:c.1112C>G
|
NP_000519.2:p.Ser371Ter
|
|
NM_001173498.1:c.1109C>G
|
NP_001166969.1:p.Ser370Ter
|
|
XM_005259913.1:c.1115C>G
|
XP_005259970.1:p.Ser372Ter
|
|
XM_011528017.1:c.11C>G
|
XP_011526319.1:p.Ser4Ter
|
|
XM_005259913.2:c.1115C>G
|
XP_005259970.1:p.Ser372Ter
|
|
XM_024451518.1:c.11C>G
|
XP_024307286.1:p.Ser4Ter
|
|
NM_000528.4:c.1112C>G
MANE Select
|
NP_000519.2:p.Ser371Ter
|
|
NM_001173498.2:c.1109C>G
|
NP_001166969.1:p.Ser370Ter
|
|