ENST00000559133.6:c.*1258T>G
|
ENSP00000453958.2:n.*1258T>G
|
|
ENST00000674301.2:c.*1963T>G
|
ENSP00000501333.2:n.*1963T>G
|
|
ENST00000682158.1:n.1831T>G
|
|
|
ENST00000682170.1:n.2631T>G
|
|
|
ENST00000682767.1:n.1747T>G
|
|
|
ENST00000316623.10:c.8450T>G
MANE Select
|
ENSP00000325527.5:p.Phe2817Cys
|
|
ENST00000674301.1:c.3616T>G
|
ENSP00000501333.1:n.3616T>G
|
|
ENST00000316623.9:c.8450T>G
|
ENSP00000325527.5:p.Phe2817Cys
|
|
ENST00000559133.5:c.3819T>G
|
|
|
NM_000138.4:c.8450T>G , LRG_778t1:c.8450T>G
|
NP_000129.3:p.Phe2817Cys
|
|
NM_000138.5:c.8450T>G
MANE Select
|
NP_000129.3:p.Phe2817Cys
|
|