ENST00000307998.11:c.1212G>A
(EFEMP2)
MANE Select
|
ENSP00000309953.6:p.Pro404=
|
|
ENST00000307998.10:c.1212G>A
(EFEMP2)
|
ENSP00000309953.6:p.Pro404=
|
|
ENST00000524408.1:c.88G>A
(EFEMP2)
|
|
|
ENST00000525006.1:n.38-219C>T
(MUS81)
|
|
|
ENST00000526628.5:n.1778G>A
(EFEMP2)
|
|
|
ENST00000526911.1:c.189G>A
(EFEMP2)
|
ENSP00000436536.1:p.Pro63=
|
|
ENST00000527277.5:c.43G>A
(EFEMP2)
|
|
|
ENST00000528176.5:c.1171-326G>A
(EFEMP2)
|
ENSP00000434151.1:n.1171-326G>A
|
|
ENST00000528409.1:n.445G>A
(EFEMP2)
|
|
|
ENST00000530806.5:c.171G>A
(EFEMP2)
|
ENSP00000436526.1:p.Pro57=
|
|
ENST00000531645.5:c.319-104G>A
(EFEMP2)
|
ENSP00000436521.1:n.319-104G>A
|
|
ENST00000531972.5:c.1212G>A
(EFEMP2)
|
ENSP00000435295.1:p.Pro404=
|
|
ENST00000532648.1:n.67G>A
(EFEMP2)
|
|
|
NM_016938.4:c.1212G>A
(EFEMP2)
|
NP_058634.4:p.Pro404=
|
|
NR_037718.1:n.1471G>A
(EFEMP2)
|
|
|
NR_146598.1:n.1845-219C>T
(MUS81)
|
|
|
NM_016938.5:c.1212G>A
(EFEMP2)
MANE Select
|
NP_058634.4:p.Pro404=
|
|
NR_037718.2:n.1337G>A
(EFEMP2)
|
|
|
NR_146598.2:n.1813-219C>T
(MUS81)
|
|
|