|
NM_000138.5:c.7921C>T
MANE Select
|
NP_000129.3:p.Gln2641Ter
|
|
ENST00000316623.10:c.7921C>T
MANE Select
|
ENSP00000325527.5:p.Gln2641Ter
|
|
NM_000138.4:c.7921C>T , LRG_778t1:c.7921C>T
|
NP_000129.3:p.Gln2641Ter
|
|
ENST00000316623.9:c.7921C>T
|
ENSP00000325527.5:p.Gln2641Ter
|
|
ENST00000559133.5:c.3290C>T
|
|
|
ENST00000559133.6:c.*729C>T
|
ENSP00000453958.2:n.*729C>T
|
|
ENST00000561429.1:n.176C>T
|
|
|
ENST00000674301.1:c.3087C>T
|
ENSP00000501333.1:n.3087C>T
|
|
ENST00000674301.2:c.*1434C>T
|
ENSP00000501333.2:n.*1434C>T
|
|
ENST00000682158.1:n.1302C>T
|
|
|
ENST00000682170.1:n.2102C>T
|
|
|
ENST00000682767.1:n.1218C>T
|
|