ENST00000559133.6:c.*1081T>A
|
ENSP00000453958.2:n.*1081T>A
|
|
ENST00000674301.2:c.*1786T>A
|
ENSP00000501333.2:n.*1786T>A
|
|
ENST00000682158.1:n.1654T>A
|
|
|
ENST00000682170.1:n.2454T>A
|
|
|
ENST00000682767.1:n.1570T>A
|
|
|
ENST00000316623.10:c.8273T>A
MANE Select
|
ENSP00000325527.5:p.Val2758Asp
|
|
ENST00000674301.1:c.3439T>A
|
ENSP00000501333.1:n.3439T>A
|
|
ENST00000316623.9:c.8273T>A
|
ENSP00000325527.5:p.Val2758Asp
|
|
ENST00000559133.5:c.3642T>A
|
|
|
ENST00000561429.1:n.528T>A
|
|
|
NM_000138.4:c.8273T>A , LRG_778t1:c.8273T>A
|
NP_000129.3:p.Val2758Asp
|
|
NM_000138.5:c.8273T>A
MANE Select
|
NP_000129.3:p.Val2758Asp
|
|