ENST00000559133.6:c.*824T>G
|
ENSP00000453958.2:n.*824T>G
|
|
ENST00000674301.2:c.*1529T>G
|
ENSP00000501333.2:n.*1529T>G
|
|
ENST00000682158.1:n.1397T>G
|
|
|
ENST00000682170.1:n.2197T>G
|
|
|
ENST00000682767.1:n.1313T>G
|
|
|
ENST00000316623.10:c.8016T>G
MANE Select
|
ENSP00000325527.5:p.Cys2672Trp
|
|
ENST00000674301.1:c.3182T>G
|
ENSP00000501333.1:n.3182T>G
|
|
ENST00000316623.9:c.8016T>G
|
ENSP00000325527.5:p.Cys2672Trp
|
|
ENST00000559133.5:c.3385T>G
|
|
|
ENST00000561429.1:n.271T>G
|
|
|
NM_000138.4:c.8016T>G , LRG_778t1:c.8016T>G
|
NP_000129.3:p.Cys2672Trp
|
|
NM_000138.5:c.8016T>G
MANE Select
|
NP_000129.3:p.Cys2672Trp
|
|