ENST00000253122.10:c.1152_1156dup
MANE Select
|
ENSP00000253122.5:p.Phe386TrpfsTer12
|
|
ENST00000253122.9:c.1152_1156dup
|
ENSP00000253122.5:p.Phe386TrpfsTer12
|
|
ENST00000413787.1:c.258-289_258-285dup
|
ENSP00000400463.1:n.258-289_258-285dup
|
|
ENST00000430077.6:c.807_811dup
|
ENSP00000403041.2:p.Phe271TrpfsTer12
|
|
ENST00000442457.1:c.206_210dup
|
|
|
ENST00000457723.1:c.136_140dup
|
ENSP00000394742.1:p.His48AlafsTer?
|
|
ENST00000467402.1:n.251_255dup
|
|
|
ENST00000485324.1:n.1185_1189dup
|
|
|
NM_001142805.1:c.1122_1126dup
|
NP_001136277.1:p.Phe376TrpfsTer12
|
|
NM_001142806.1:c.807_811dup
|
NP_001136278.1:p.Phe271TrpfsTer12
|
|
NM_005629.3:c.1152_1156dup
|
NP_005620.1:p.Phe386TrpfsTer12
|
|
NM_005629.4:c.1152_1156dup
MANE Select
|
NP_005620.1:p.Phe386TrpfsTer12
|
|
NM_001142805.2:c.1122_1126dup
|
NP_001136277.1:p.Phe376TrpfsTer12
|
|