ENST00000559133.6:c.*1288A>G
|
ENSP00000453958.2:n.*1288A>G
|
|
ENST00000674301.2:c.*1993A>G
|
ENSP00000501333.2:n.*1993A>G
|
|
ENST00000682158.1:n.1861A>G
|
|
|
ENST00000682170.1:n.2661A>G
|
|
|
ENST00000682767.1:n.1777A>G
|
|
|
ENST00000316623.10:c.8480A>G
MANE Select
|
ENSP00000325527.5:p.Tyr2827Cys
|
|
ENST00000674301.1:c.3646A>G
|
ENSP00000501333.1:n.3646A>G
|
|
ENST00000316623.9:c.8480A>G
|
ENSP00000325527.5:p.Tyr2827Cys
|
|
ENST00000559133.5:c.3849A>G
|
|
|
NM_000138.4:c.8480A>G , LRG_778t1:c.8480A>G
|
NP_000129.3:p.Tyr2827Cys
|
|
NM_000138.5:c.8480A>G
MANE Select
|
NP_000129.3:p.Tyr2827Cys
|
|