ENST00000585465.3:c.721G=
|
ENSP00000490268.2:p.Ala241=
|
|
ENST00000585748.3:c.349G=
|
ENSP00000477641.2:p.Ala117=
|
|
ENST00000585851.2:c.547G=
|
ENSP00000467912.2:p.Ala183=
|
|
ENST00000326873.12:c.721G=
MANE Select
|
ENSP00000324856.6:p.Ala241=
|
|
ENST00000652231.1:c.721G=
|
ENSP00000498804.1:p.Ala241=
|
|
ENST00000326873.11:c.721G=
|
ENSP00000324856.6:p.Ala241=
|
|
ENST00000586243.5:c.721G=
|
ENSP00000467240.2:p.Ala241=
|
|
ENST00000586358.5:n.619G=
|
|
|
ENST00000589152.5:n.811G=
|
|
|
ENST00000591133.2:n.692G=
|
|
|
NM_000455.4:c.721G= , LRG_319t1:c.721G=
|
NP_000446.1:p.Ala241=
|
|
XM_005259617.1:c.721G=
|
XP_005259674.1:p.Ala241=
|
|
XM_005259618.3:c.721G=
|
XP_005259675.1:p.Ala241=
|
|
XM_011528209.1:c.499G=
|
XP_011526511.1:p.Ala167=
|
|
XR_936204.1:n.1346G=
|
|
|
XM_005259617.3:c.721G=
|
XP_005259674.1:p.Ala241=
|
|
XM_011528209.2:c.499G=
|
XP_011526511.1:p.Ala167=
|
|
XR_001753738.2:n.1346G=
|
|
|
XR_001753739.1:n.1346G=
|
|
|
XR_001753740.2:n.1346G=
|
|
|
NM_000455.5:c.721G=
MANE Select
|
NP_000446.1:p.Ala241=
|
|