ENST00000585465.3:c.*2767C>G
|
ENSP00000490268.2:n.*2767C>G
|
|
ENST00000585748.3:c.794C>G
|
ENSP00000477641.2:p.Ala265Gly
|
|
ENST00000585851.2:c.992C>G
|
ENSP00000467912.2:p.Ala331Gly
|
|
ENST00000326873.12:c.1166C>G
MANE Select
|
ENSP00000324856.6:p.Ala389Gly
|
|
ENST00000326873.11:c.1166C>G
|
ENSP00000324856.6:p.Ala389Gly
|
|
ENST00000585465.2:n.2899C>G
|
|
|
ENST00000586243.5:c.1166C>G
|
ENSP00000467240.2:p.Ala389Gly
|
|
ENST00000589152.5:n.1864C>G
|
|
|
NM_000455.4:c.1166C>G , LRG_319t1:c.1166C>G
|
NP_000446.1:p.Ala389Gly
|
|
XM_005259617.1:c.1161C>G
|
XP_005259674.1:p.Gly387=
|
|
XM_011528209.1:c.939C>G
|
XP_011526511.1:p.Gly313=
|
|
XM_005259617.3:c.1161C>G
|
XP_005259674.1:p.Gly387=
|
|
XM_011528209.2:c.939C>G
|
XP_011526511.1:p.Gly313=
|
|
XR_001753738.2:n.1972C>G
|
|
|
XR_001753740.2:n.1942C>G
|
|
|
NM_000455.5:c.1166C>G
MANE Select
|
NP_000446.1:p.Ala389Gly
|
|