ENST00000559133.6:c.*790A>G
|
ENSP00000453958.2:n.*790A>G
|
|
ENST00000674301.2:c.*1495A>G
|
ENSP00000501333.2:n.*1495A>G
|
|
ENST00000682158.1:n.1363A>G
|
|
|
ENST00000682170.1:n.2163A>G
|
|
|
ENST00000682767.1:n.1279A>G
|
|
|
ENST00000316623.10:c.7982A>G
MANE Select
|
ENSP00000325527.5:p.Tyr2661Cys
|
|
ENST00000674301.1:c.3148A>G
|
ENSP00000501333.1:n.3148A>G
|
|
ENST00000316623.9:c.7982A>G
|
ENSP00000325527.5:p.Tyr2661Cys
|
|
ENST00000559133.5:c.3351A>G
|
|
|
ENST00000561429.1:n.237A>G
|
|
|
NM_000138.4:c.7982A>G , LRG_778t1:c.7982A>G
|
NP_000129.3:p.Tyr2661Cys
|
|
NM_000138.5:c.7982A>G
MANE Select
|
NP_000129.3:p.Tyr2661Cys
|
|