ENST00000559133.6:c.*1013A>T
|
ENSP00000453958.2:n.*1013A>T
|
|
ENST00000674301.2:c.*1718A>T
|
ENSP00000501333.2:n.*1718A>T
|
|
ENST00000682158.1:n.1586A>T
|
|
|
ENST00000682170.1:n.2386A>T
|
|
|
ENST00000682767.1:n.1502A>T
|
|
|
ENST00000316623.10:c.8205A>T
MANE Select
|
ENSP00000325527.5:p.Glu2735Asp
|
|
ENST00000674301.1:c.3371A>T
|
ENSP00000501333.1:n.3371A>T
|
|
ENST00000316623.9:c.8205A>T
|
ENSP00000325527.5:p.Glu2735Asp
|
|
ENST00000559133.5:c.3574A>T
|
|
|
ENST00000561429.1:n.460A>T
|
|
|
NM_000138.4:c.8205A>T , LRG_778t1:c.8205A>T
|
NP_000129.3:p.Glu2735Asp
|
|
NM_000138.5:c.8205A>T
MANE Select
|
NP_000129.3:p.Glu2735Asp
|
|