ENST00000585465.3:c.*2882G>C
|
ENSP00000490268.2:n.*2882G>C
|
|
ENST00000585748.3:c.909G>C
|
ENSP00000477641.2:p.Leu303=
|
|
ENST00000585851.2:c.1107G>C
|
ENSP00000467912.2:p.Leu369=
|
|
ENST00000326873.12:c.1281G>C
MANE Select
|
ENSP00000324856.6:p.Leu427=
|
|
ENST00000326873.11:c.1281G>C
|
ENSP00000324856.6:p.Leu427=
|
|
ENST00000585465.2:n.3014G>C
|
|
|
ENST00000586243.5:c.1278G>C
|
ENSP00000467240.2:p.Leu426=
|
|
ENST00000589152.5:n.1979G>C
|
|
|
NM_000455.4:c.1281G>C , LRG_319t1:c.1281G>C
|
NP_000446.1:p.Leu427=
|
|
XM_005259617.1:c.1276G>C
|
XP_005259674.1:p.Val426Leu
|
|
XM_011528209.1:c.1054G>C
|
XP_011526511.1:p.Val352Leu
|
|
XM_005259617.3:c.1276G>C
|
XP_005259674.1:p.Val426Leu
|
|
XM_011528209.2:c.1054G>C
|
XP_011526511.1:p.Val352Leu
|
|
XR_001753738.2:n.2087G>C
|
|
|
XR_001753740.2:n.2057G>C
|
|
|
NM_000455.5:c.1281G>C
MANE Select
|
NP_000446.1:p.Leu427=
|
|