ENST00000585465.3:c.*2824G>T
|
ENSP00000490268.2:n.*2824G>T
|
|
ENST00000585748.3:c.851G>T
|
ENSP00000477641.2:p.Gly284Val
|
|
ENST00000585851.2:c.1049G>T
|
ENSP00000467912.2:p.Gly350Val
|
|
ENST00000326873.12:c.1223G>T
MANE Select
|
ENSP00000324856.6:p.Gly408Val
|
|
ENST00000326873.11:c.1223G>T
|
ENSP00000324856.6:p.Gly408Val
|
|
ENST00000585465.2:n.2956G>T
|
|
|
ENST00000586243.5:c.1222G>T
|
ENSP00000467240.2:p.Ala408Ser
|
|
ENST00000589152.5:n.1921G>T
|
|
|
NM_000455.4:c.1223G>T , LRG_319t1:c.1223G>T
|
NP_000446.1:p.Gly408Val
|
|
XM_005259617.1:c.1218G>T
|
XP_005259674.1:p.Gly406=
|
|
XM_011528209.1:c.996G>T
|
XP_011526511.1:p.Gly332=
|
|
XM_005259617.3:c.1218G>T
|
XP_005259674.1:p.Gly406=
|
|
XM_011528209.2:c.996G>T
|
XP_011526511.1:p.Gly332=
|
|
XR_001753738.2:n.2029G>T
|
|
|
XR_001753740.2:n.1999G>T
|
|
|
NM_000455.5:c.1223G>T
MANE Select
|
NP_000446.1:p.Gly408Val
|
|