ENST00000559133.6:c.*1081T>G
|
ENSP00000453958.2:n.*1081T>G
|
|
ENST00000674301.2:c.*1786T>G
|
ENSP00000501333.2:n.*1786T>G
|
|
ENST00000682158.1:n.1654T>G
|
|
|
ENST00000682170.1:n.2454T>G
|
|
|
ENST00000682767.1:n.1570T>G
|
|
|
ENST00000316623.10:c.8273T>G
MANE Select
|
ENSP00000325527.5:p.Val2758Gly
|
|
ENST00000674301.1:c.3439T>G
|
ENSP00000501333.1:n.3439T>G
|
|
ENST00000316623.9:c.8273T>G
|
ENSP00000325527.5:p.Val2758Gly
|
|
ENST00000559133.5:c.3642T>G
|
|
|
ENST00000561429.1:n.528T>G
|
|
|
NM_000138.4:c.8273T>G , LRG_778t1:c.8273T>G
|
NP_000129.3:p.Val2758Gly
|
|
NM_000138.5:c.8273T>G
MANE Select
|
NP_000129.3:p.Val2758Gly
|
|