|
NM_002317.7:c.915C>T
(LOX)
MANE Select
|
NP_002308.2:p.Asp305=
|
|
ENST00000231004.5:c.915C>T
(LOX)
MANE Select
|
ENSP00000231004.4:p.Asp305=
|
|
NM_001178102.1:c.225C>T
(LOX)
|
NP_001171573.1:p.Asp75=
|
|
NM_001178102.2:c.225C>T
(LOX)
|
NP_001171573.1:p.Asp75=
|
|
NM_001317073.1:c.24C>T
(LOX)
|
NP_001304002.1:p.Asp8=
|
|
NM_002317.5:c.915C>T
(LOX)
|
NP_002308.2:p.Asp305=
|
|
NM_002317.6:c.915C>T
(LOX)
|
NP_002308.2:p.Asp305=
|
|
ENST00000231004.4:c.915C>T
(LOX)
|
ENSP00000231004.4:p.Asp305=
|
|
ENST00000503759.5:n.506C>T
(LOX)
|
|
|
ENST00000504881.1:n.312-1182G>A
(SRFBP1)
|
|
|
ENST00000505593.5:n.241C>T
(LOX)
|
|
|
ENST00000508067.1:c.293C>T
(LOX)
|
ENSP00000427538.1:n.293C>T
|
|
ENST00000513319.5:n.258C>T
(LOX)
|
|
|
ENST00000639739.2:c.*107C>T
(LOX)
|
ENSP00000492324.2:n.*107C>T
|
|
XM_017009111.2:c.1106-1182G>A
(SRFBP1)
|
XP_016864600.2:n.1106-1182G>A
|
