ENST00000559133.6:c.*766G>A
|
ENSP00000453958.2:n.*766G>A
|
|
ENST00000674301.2:c.*1471G>A
|
ENSP00000501333.2:n.*1471G>A
|
|
ENST00000682158.1:n.1339G>A
|
|
|
ENST00000682170.1:n.2139G>A
|
|
|
ENST00000682767.1:n.1255G>A
|
|
|
ENST00000316623.10:c.7958G>A
MANE Select
|
ENSP00000325527.5:p.Gly2653Asp
|
|
ENST00000674301.1:c.3124G>A
|
ENSP00000501333.1:n.3124G>A
|
|
ENST00000316623.9:c.7958G>A
|
ENSP00000325527.5:p.Gly2653Asp
|
|
ENST00000559133.5:c.3327G>A
|
|
|
ENST00000561429.1:n.213G>A
|
|
|
NM_000138.4:c.7958G>A , LRG_778t1:c.7958G>A
|
NP_000129.3:p.Gly2653Asp
|
|
NM_000138.5:c.7958G>A
MANE Select
|
NP_000129.3:p.Gly2653Asp
|
|