ENST00000559133.6:c.*695C>G
|
ENSP00000453958.2:n.*695C>G
|
|
ENST00000674301.2:c.*1400C>G
|
ENSP00000501333.2:n.*1400C>G
|
|
ENST00000682158.1:n.1268C>G
|
|
|
ENST00000682170.1:n.2068C>G
|
|
|
ENST00000682767.1:n.1184C>G
|
|
|
ENST00000316623.10:c.7887C>G
MANE Select
|
ENSP00000325527.5:p.Tyr2629Ter
|
|
ENST00000674301.1:c.3053C>G
|
ENSP00000501333.1:n.3053C>G
|
|
ENST00000316623.9:c.7887C>G
|
ENSP00000325527.5:p.Tyr2629Ter
|
|
ENST00000559133.5:c.3256C>G
|
|
|
ENST00000561429.1:n.142C>G
|
|
|
NM_000138.4:c.7887C>G , LRG_778t1:c.7887C>G
|
NP_000129.3:p.Tyr2629Ter
|
|
NM_000138.5:c.7887C>G
MANE Select
|
NP_000129.3:p.Tyr2629Ter
|
|