ENST00000585465.3:c.*2866_*2868del
|
ENSP00000490268.2:n.*2866_*2868del
|
|
ENST00000585748.3:c.893_895del
|
ENSP00000477641.2:p.Ser298del
|
|
ENST00000585851.2:c.1091_1093del
|
ENSP00000467912.2:p.Ser364del
|
|
ENST00000326873.12:c.1265_1267del
MANE Select
|
ENSP00000324856.6:p.Ser422del
|
|
ENST00000326873.11:c.1265_1267del
|
ENSP00000324856.6:p.Ser422del
|
|
ENST00000585465.2:n.2998_3000del
|
|
|
ENST00000586243.5:c.1262_1264del
|
ENSP00000467240.2:p.Ser421del
|
|
ENST00000589152.5:n.1963_1965del
|
|
|
NM_000455.4:c.1265_1267del , LRG_319t1:c.1265_1267del
|
NP_000446.1:p.Ser422del
|
|
XM_005259617.1:c.1260_1262del
|
XP_005259674.1:p.Gln421del
|
|
XM_011528209.1:c.1038_1040del
|
XP_011526511.1:p.Gln347del
|
|
XM_005259617.3:c.1260_1262del
|
XP_005259674.1:p.Gln421del
|
|
XM_011528209.2:c.1038_1040del
|
XP_011526511.1:p.Gln347del
|
|
XR_001753738.2:n.2071_2073del
|
|
|
XR_001753740.2:n.2041_2043del
|
|
|
NM_000455.5:c.1265_1267del
MANE Select
|
NP_000446.1:p.Ser422del
|
|