ENST00000585465.3:c.*2829G>A
|
ENSP00000490268.2:n.*2829G>A
|
|
ENST00000585748.3:c.856G>A
|
ENSP00000477641.2:p.Ala286Thr
|
|
ENST00000585851.2:c.1054G>A
|
ENSP00000467912.2:p.Ala352Thr
|
|
ENST00000326873.12:c.1228G>A
MANE Select
|
ENSP00000324856.6:p.Ala410Thr
|
|
ENST00000326873.11:c.1228G>A
|
ENSP00000324856.6:p.Ala410Thr
|
|
ENST00000585465.2:n.2961G>A
|
|
|
ENST00000586243.5:c.1227G>A
|
ENSP00000467240.2:p.Gly409=
|
|
ENST00000589152.5:n.1926G>A
|
|
|
NM_000455.4:c.1228G>A , LRG_319t1:c.1228G>A
|
NP_000446.1:p.Ala410Thr
|
|
XM_005259617.1:c.1223G>A
|
XP_005259674.1:p.Gly408Asp
|
|
XM_011528209.1:c.1001G>A
|
XP_011526511.1:p.Gly334Asp
|
|
XM_005259617.3:c.1223G>A
|
XP_005259674.1:p.Gly408Asp
|
|
XM_011528209.2:c.1001G>A
|
XP_011526511.1:p.Gly334Asp
|
|
XR_001753738.2:n.2034G>A
|
|
|
XR_001753740.2:n.2004G>A
|
|
|
NM_000455.5:c.1228G>A
MANE Select
|
NP_000446.1:p.Ala410Thr
|
|