ENST00000585465.3:c.*2742G>C
|
ENSP00000490268.2:n.*2742G>C
|
|
ENST00000585748.3:c.769G>C
|
ENSP00000477641.2:p.Gly257Arg
|
|
ENST00000585851.2:c.967G>C
|
ENSP00000467912.2:p.Gly323Arg
|
|
ENST00000326873.12:c.1141G>C
MANE Select
|
ENSP00000324856.6:p.Gly381Arg
|
|
ENST00000326873.11:c.1141G>C
|
ENSP00000324856.6:p.Gly381Arg
|
|
ENST00000585465.2:n.2874G>C
|
|
|
ENST00000586243.5:c.1141G>C
|
ENSP00000467240.2:p.Gly381Arg
|
|
ENST00000589152.5:n.1839G>C
|
|
|
NM_000455.4:c.1141G>C , LRG_319t1:c.1141G>C
|
NP_000446.1:p.Gly381Arg
|
|
XM_005259617.1:c.1136G>C
|
XP_005259674.1:p.Trp379Ser
|
|
XM_011528209.1:c.914G>C
|
XP_011526511.1:p.Trp305Ser
|
|
XM_005259617.3:c.1136G>C
|
XP_005259674.1:p.Trp379Ser
|
|
XM_011528209.2:c.914G>C
|
XP_011526511.1:p.Trp305Ser
|
|
XR_001753738.2:n.1947G>C
|
|
|
XR_001753740.2:n.1917G>C
|
|
|
NM_000455.5:c.1141G>C
MANE Select
|
NP_000446.1:p.Gly381Arg
|
|