ENST00000585465.3:c.*2815G>C
|
ENSP00000490268.2:n.*2815G>C
|
|
ENST00000585748.3:c.842G>C
|
ENSP00000477641.2:p.Arg281Thr
|
|
ENST00000585851.2:c.1040G>C
|
ENSP00000467912.2:p.Arg347Thr
|
|
ENST00000326873.12:c.1214G>C
MANE Select
|
ENSP00000324856.6:p.Arg405Thr
|
|
ENST00000326873.11:c.1214G>C
|
ENSP00000324856.6:p.Arg405Thr
|
|
ENST00000585465.2:n.2947G>C
|
|
|
ENST00000586243.5:c.1214G>C
|
ENSP00000467240.2:p.Arg405Thr
|
|
ENST00000589152.5:n.1912G>C
|
|
|
NM_000455.4:c.1214G>C , LRG_319t1:c.1214G>C
|
NP_000446.1:p.Arg405Thr
|
|
XM_005259617.1:c.1209G>C
|
XP_005259674.1:p.Gln403His
|
|
XM_011528209.1:c.987G>C
|
XP_011526511.1:p.Gln329His
|
|
XM_005259617.3:c.1209G>C
|
XP_005259674.1:p.Gln403His
|
|
XM_011528209.2:c.987G>C
|
XP_011526511.1:p.Gln329His
|
|
XR_001753738.2:n.2020G>C
|
|
|
XR_001753740.2:n.1990G>C
|
|
|
NM_000455.5:c.1214G>C
MANE Select
|
NP_000446.1:p.Arg405Thr
|
|