ENST00000559133.6:c.*1183G>A
|
ENSP00000453958.2:n.*1183G>A
|
|
ENST00000674301.2:c.*1888G>A
|
ENSP00000501333.2:n.*1888G>A
|
|
ENST00000682158.1:n.1756G>A
|
|
|
ENST00000682170.1:n.2556G>A
|
|
|
ENST00000682767.1:n.1672G>A
|
|
|
ENST00000316623.10:c.8375G>A
MANE Select
|
ENSP00000325527.5:p.Arg2792Lys
|
|
ENST00000674301.1:c.3541G>A
|
ENSP00000501333.1:n.3541G>A
|
|
ENST00000316623.9:c.8375G>A
|
ENSP00000325527.5:p.Arg2792Lys
|
|
ENST00000559133.5:c.3744G>A
|
|
|
ENST00000561429.1:n.630G>A
|
|
|
NM_000138.4:c.8375G>A , LRG_778t1:c.8375G>A
|
NP_000129.3:p.Arg2792Lys
|
|
NM_000138.5:c.8375G>A
MANE Select
|
NP_000129.3:p.Arg2792Lys
|
|