ENST00000585465.3:c.*2881T>G
|
ENSP00000490268.2:n.*2881T>G
|
|
ENST00000585748.3:c.908T>G
|
ENSP00000477641.2:p.Leu303Arg
|
|
ENST00000585851.2:c.1106T>G
|
ENSP00000467912.2:p.Leu369Arg
|
|
ENST00000326873.12:c.1280T>G
MANE Select
|
ENSP00000324856.6:p.Leu427Arg
|
|
ENST00000326873.11:c.1280T>G
|
ENSP00000324856.6:p.Leu427Arg
|
|
ENST00000585465.2:n.3013T>G
|
|
|
ENST00000586243.5:c.1277T>G
|
ENSP00000467240.2:p.Leu426Arg
|
|
ENST00000589152.5:n.1978T>G
|
|
|
NM_000455.4:c.1280T>G , LRG_319t1:c.1280T>G
|
NP_000446.1:p.Leu427Arg
|
|
XM_005259617.1:c.1275T>G
|
XP_005259674.1:p.Ala425=
|
|
XM_011528209.1:c.1053T>G
|
XP_011526511.1:p.Ala351=
|
|
XM_005259617.3:c.1275T>G
|
XP_005259674.1:p.Ala425=
|
|
XM_011528209.2:c.1053T>G
|
XP_011526511.1:p.Ala351=
|
|
XR_001753738.2:n.2086T>G
|
|
|
XR_001753740.2:n.2056T>G
|
|
|
NM_000455.5:c.1280T>G
MANE Select
|
NP_000446.1:p.Leu427Arg
|
|