ENST00000585465.3:c.*2715G>C
|
ENSP00000490268.2:n.*2715G>C
|
|
ENST00000585748.3:c.742G>C
|
ENSP00000477641.2:p.Val248Leu
|
|
ENST00000585851.2:c.940G>C
|
ENSP00000467912.2:p.Val314Leu
|
|
ENST00000326873.12:c.1114G>C
MANE Select
|
ENSP00000324856.6:p.Val372Leu
|
|
ENST00000326873.11:c.1114G>C
|
ENSP00000324856.6:p.Val372Leu
|
|
ENST00000585465.2:n.2847G>C
|
|
|
ENST00000586243.5:c.1114G>C
|
ENSP00000467240.2:p.Val372Leu
|
|
ENST00000589152.5:n.1812G>C
|
|
|
NM_000455.4:c.1114G>C , LRG_319t1:c.1114G>C
|
NP_000446.1:p.Val372Leu
|
|
XM_005259617.1:c.1109G>C
|
XP_005259674.1:p.Gly370Ala
|
|
XM_011528209.1:c.887G>C
|
XP_011526511.1:p.Gly296Ala
|
|
XM_005259617.3:c.1109G>C
|
XP_005259674.1:p.Gly370Ala
|
|
XM_011528209.2:c.887G>C
|
XP_011526511.1:p.Gly296Ala
|
|
XR_001753738.2:n.1920G>C
|
|
|
XR_001753740.2:n.1890G>C
|
|
|
NM_000455.5:c.1114G>C
MANE Select
|
NP_000446.1:p.Val372Leu
|
|