ENST00000559133.6:c.*1317T>G
|
ENSP00000453958.2:n.*1317T>G
|
|
ENST00000674301.2:c.*2022T>G
|
ENSP00000501333.2:n.*2022T>G
|
|
ENST00000682158.1:n.1890T>G
|
|
|
ENST00000682170.1:n.2690T>G
|
|
|
ENST00000682767.1:n.1806T>G
|
|
|
ENST00000316623.10:c.8509T>G
MANE Select
|
ENSP00000325527.5:p.Tyr2837Asp
|
|
ENST00000674301.1:c.3675T>G
|
ENSP00000501333.1:n.3675T>G
|
|
ENST00000316623.9:c.8509T>G
|
ENSP00000325527.5:p.Tyr2837Asp
|
|
ENST00000559133.5:c.3878T>G
|
|
|
NM_000138.4:c.8509T>G , LRG_778t1:c.8509T>G
|
NP_000129.3:p.Tyr2837Asp
|
|
NM_000138.5:c.8509T>G
MANE Select
|
NP_000129.3:p.Tyr2837Asp
|
|