ENST00000231004.5:c.1188G>T
(LOX)
MANE Select
|
ENSP00000231004.4:p.Val396=
|
|
ENST00000639739.2:c.*380G>T
(LOX)
|
ENSP00000492324.2:n.*380G>T
|
|
ENST00000231004.4:c.1188G>T
(LOX)
|
ENSP00000231004.4:p.Val396=
|
|
ENST00000503759.5:n.779G>T
(LOX)
|
|
|
ENST00000504881.1:n.312-5203C>A
(SRFBP1)
|
|
|
ENST00000505593.5:n.514G>T
(LOX)
|
|
|
ENST00000513319.5:n.531G>T
(LOX)
|
|
|
NM_001178102.1:c.498G>T
(LOX)
|
NP_001171573.1:p.Val166=
|
|
NM_001178102.2:c.498G>T
(LOX)
|
NP_001171573.1:p.Val166=
|
|
NM_001317073.1:c.297G>T
(LOX)
|
NP_001304002.1:p.Val99=
|
|
NM_002317.5:c.1188G>T
(LOX)
|
NP_002308.2:p.Val396=
|
|
NM_002317.6:c.1188G>T
(LOX)
|
NP_002308.2:p.Val396=
|
|
XM_017009111.2:c.1106-5203C>A
(SRFBP1)
|
XP_016864600.2:n.1106-5203C>A
|
|
NM_002317.7:c.1188G>T
(LOX)
MANE Select
|
NP_002308.2:p.Val396=
|
|