ENST00000585465.3:c.*2853_*2854del
|
ENSP00000490268.2:n.*2853_*2854del
|
|
ENST00000585748.3:c.880_881del
|
ENSP00000477641.2:p.Cys294LeufsTer?
|
|
ENST00000585851.2:c.1078_1079del
|
ENSP00000467912.2:p.Cys360LeufsTer?
|
|
ENST00000326873.12:c.1252_1253del
MANE Select
|
ENSP00000324856.6:p.Cys418LeufsTer?
|
|
ENST00000326873.11:c.1252_1253del
|
ENSP00000324856.6:p.Cys418LeufsTer?
|
|
ENST00000585465.2:n.2985_2986del
|
|
|
ENST00000586243.5:c.1251_1252del
|
ENSP00000467240.2:p.Ala418CysfsTer?
|
|
ENST00000589152.5:n.1950_1951del
|
|
|
NM_000455.4:c.1252_1253del , LRG_319t1:c.1252_1253del
|
NP_000446.1:p.Cys418LeufsTer?
|
|
XM_005259617.1:c.1247_1248del
|
XP_005259674.1:p.Leu416ProfsTer?
|
|
XM_011528209.1:c.1025_1026del
|
XP_011526511.1:p.Leu342ProfsTer?
|
|
XM_005259617.3:c.1247_1248del
|
XP_005259674.1:p.Leu416ProfsTer?
|
|
XM_011528209.2:c.1025_1026del
|
XP_011526511.1:p.Leu342ProfsTer?
|
|
XR_001753738.2:n.2058_2059del
|
|
|
XR_001753740.2:n.2028_2029del
|
|
|
NM_000455.5:c.1252_1253del
MANE Select
|
NP_000446.1:p.Cys418LeufsTer?
|
|