ENST00000559133.6:c.*887C>G
|
ENSP00000453958.2:n.*887C>G
|
|
ENST00000674301.2:c.*1592C>G
|
ENSP00000501333.2:n.*1592C>G
|
|
ENST00000682158.1:n.1460C>G
|
|
|
ENST00000682170.1:n.2260C>G
|
|
|
ENST00000682767.1:n.1376C>G
|
|
|
ENST00000316623.10:c.8079C>G
MANE Select
|
ENSP00000325527.5:p.Gly2693=
|
|
ENST00000674301.1:c.3245C>G
|
ENSP00000501333.1:n.3245C>G
|
|
ENST00000316623.9:c.8079C>G
|
ENSP00000325527.5:p.Gly2693=
|
|
ENST00000559133.5:c.3448C>G
|
|
|
ENST00000561429.1:n.334C>G
|
|
|
NM_000138.4:c.8079C>G , LRG_778t1:c.8079C>G
|
NP_000129.3:p.Gly2693=
|
|
NM_000138.5:c.8079C>G
MANE Select
|
NP_000129.3:p.Gly2693=
|
|