ENST00000585465.3:c.*2891C>G
|
ENSP00000490268.2:n.*2891C>G
|
|
ENST00000585748.3:c.918C>G
|
ENSP00000477641.2:p.Cys306Trp
|
|
ENST00000585851.2:c.1116C>G
|
ENSP00000467912.2:p.Cys372Trp
|
|
ENST00000326873.12:c.1290C>G
MANE Select
|
ENSP00000324856.6:p.Cys430Trp
|
|
ENST00000326873.11:c.1290C>G
|
ENSP00000324856.6:p.Cys430Trp
|
|
ENST00000585465.2:n.3023C>G
|
|
|
ENST00000586243.5:c.1287C>G
|
ENSP00000467240.2:p.Cys429Trp
|
|
ENST00000589152.5:n.1988C>G
|
|
|
NM_000455.4:c.1290C>G , LRG_319t1:c.1290C>G
|
NP_000446.1:p.Cys430Trp
|
|
XM_005259617.1:c.1285C>G
|
XP_005259674.1:p.Gln429Glu
|
|
XM_011528209.1:c.1063C>G
|
XP_011526511.1:p.Gln355Glu
|
|
XM_005259617.3:c.1285C>G
|
XP_005259674.1:p.Gln429Glu
|
|
XM_011528209.2:c.1063C>G
|
XP_011526511.1:p.Gln355Glu
|
|
XR_001753738.2:n.2096C>G
|
|
|
XR_001753740.2:n.2066C>G
|
|
|
NM_000455.5:c.1290C>G
MANE Select
|
NP_000446.1:p.Cys430Trp
|
|