ENST00000559133.6:c.*841dup
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ENSP00000453958.2:n.*841dup
|
|
ENST00000674301.2:c.*1546dup
|
ENSP00000501333.2:n.*1546dup
|
|
ENST00000682158.1:n.1414dup
|
|
|
ENST00000682170.1:n.2214dup
|
|
|
ENST00000682767.1:n.1330dup
|
|
|
ENST00000316623.10:c.8033dup
MANE Select
|
ENSP00000325527.5:p.Tyr2678Ter
|
|
ENST00000674301.1:c.3199dup
|
ENSP00000501333.1:n.3199dup
|
|
ENST00000316623.9:c.8033dup
|
ENSP00000325527.5:p.Tyr2678Ter
|
|
ENST00000559133.5:c.3402dup
|
|
|
ENST00000561429.1:n.288dup
|
|
|
NM_000138.4:c.8033dup , LRG_778t1:c.8033dup
|
NP_000129.3:p.Tyr2678Ter
|
|
NM_000138.5:c.8033dup
MANE Select
|
NP_000129.3:p.Tyr2678Ter
|
|