ENST00000375559.8:c.1344_1345del
MANE Select
|
ENSP00000364709.3:p.Tyr449ArgfsTer?
|
|
ENST00000375551.7:c.*335_*336del
|
ENSP00000364701.3:n.*335_*336del
|
|
ENST00000375559.7:c.1344_1345del
|
ENSP00000364709.3:p.Tyr449ArgfsTer?
|
|
ENST00000409306.5:c.*335_*336del
|
ENSP00000387092.1:n.*335_*336del
|
|
NM_000504.3:c.1344_1345del , LRG_548t1:c.1344_1345del
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NP_000495.1:p.Tyr449ArgfsTer?
|
|
NM_001312674.1:c.1212_1213del
|
NP_001299603.1:p.Tyr405ArgfsTer?
|
|
NM_001312675.1:c.*335_*336del
|
NP_001299604.1:n.*335_*336del
|
|
NM_000504.4:c.1344_1345del
MANE Select
|
NP_000495.1:p.Tyr449ArgfsTer?
|
|
NM_001312674.2:c.1212_1213del
|
NP_001299603.1:p.Tyr405ArgfsTer?
|
|
NM_001312675.2:c.*335_*336del
|
NP_001299604.1:n.*335_*336del
|
|