ENST00000231004.5:c.1189C>A
(LOX)
MANE Select
|
ENSP00000231004.4:p.Arg397Ser
|
|
ENST00000639739.2:c.*381C>A
(LOX)
|
ENSP00000492324.2:n.*381C>A
|
|
ENST00000231004.4:c.1189C>A
(LOX)
|
ENSP00000231004.4:p.Arg397Ser
|
|
ENST00000503759.5:n.780C>A
(LOX)
|
|
|
ENST00000504881.1:n.312-5204G>T
(SRFBP1)
|
|
|
ENST00000505593.5:n.515C>A
(LOX)
|
|
|
ENST00000513319.5:n.532C>A
(LOX)
|
|
|
NM_001178102.1:c.499C>A
(LOX)
|
NP_001171573.1:p.Arg167Ser
|
|
NM_001178102.2:c.499C>A
(LOX)
|
NP_001171573.1:p.Arg167Ser
|
|
NM_001317073.1:c.298C>A
(LOX)
|
NP_001304002.1:p.Arg100Ser
|
|
NM_002317.5:c.1189C>A
(LOX)
|
NP_002308.2:p.Arg397Ser
|
|
NM_002317.6:c.1189C>A
(LOX)
|
NP_002308.2:p.Arg397Ser
|
|
XM_017009111.2:c.1106-5204G>T
(SRFBP1)
|
XP_016864600.2:n.1106-5204G>T
|
|
NM_002317.7:c.1189C>A
(LOX)
MANE Select
|
NP_002308.2:p.Arg397Ser
|
|