ENST00000559133.6:c.*1125A>T
|
ENSP00000453958.2:n.*1125A>T
|
|
ENST00000674301.2:c.*1830A>T
|
ENSP00000501333.2:n.*1830A>T
|
|
ENST00000682158.1:n.1698A>T
|
|
|
ENST00000682170.1:n.2498A>T
|
|
|
ENST00000682767.1:n.1614A>T
|
|
|
ENST00000316623.10:c.8317A>T
MANE Select
|
ENSP00000325527.5:p.Asn2773Tyr
|
|
ENST00000674301.1:c.3483A>T
|
ENSP00000501333.1:n.3483A>T
|
|
ENST00000316623.9:c.8317A>T
|
ENSP00000325527.5:p.Asn2773Tyr
|
|
ENST00000559133.5:c.3686A>T
|
|
|
ENST00000561429.1:n.572A>T
|
|
|
NM_000138.4:c.8317A>T , LRG_778t1:c.8317A>T
|
NP_000129.3:p.Asn2773Tyr
|
|
NM_000138.5:c.8317A>T
MANE Select
|
NP_000129.3:p.Asn2773Tyr
|
|