|
NM_016938.5:c.*282C>T
(EFEMP2)
MANE Select
|
NP_058634.4:n.*282C>T
|
|
ENST00000307998.11:c.*282C>T
(EFEMP2)
MANE Select
|
ENSP00000309953.6:n.*282C>T
|
|
NM_016938.4:c.*282C>T
(EFEMP2)
|
NP_058634.4:n.*282C>T
|
|
NR_037718.1:n.1741C>T
(EFEMP2)
|
|
|
NR_037718.2:n.1607C>T
(EFEMP2)
|
|
|
NR_146598.1:n.1845-621G>A
(MUS81)
|
|
|
NR_146598.2:n.1813-621G>A
(MUS81)
|
|
|
ENST00000307998.10:c.*282C>T
(EFEMP2)
|
ENSP00000309953.6:n.*282C>T
|
|
ENST00000524408.1:c.337C>T
(EFEMP2)
|
|
|
ENST00000525006.1:n.38-621G>A
(MUS81)
|
|
|
ENST00000526628.5:n.2083C>T
(EFEMP2)
|
|
|
ENST00000526911.1:c.283C>T
(EFEMP2)
|
ENSP00000436536.1:n.283C>T
|
|
ENST00000527277.5:c.348C>T
(EFEMP2)
|
|
|
ENST00000528176.5:c.1247C>T
(EFEMP2)
|
ENSP00000434151.1:p.Thr416Met
|
|
ENST00000531645.5:c.485C>T
(EFEMP2)
|
ENSP00000436521.1:p.Thr162Met
|
|
ENST00000531972.5:c.*150C>T
(EFEMP2)
|
ENSP00000435295.1:n.*150C>T
|
|
ENST00000532648.1:n.337C>T
(EFEMP2)
|
|