ENST00000231004.5:c.1161T>G
(LOX)
MANE Select
|
ENSP00000231004.4:p.Pro387=
|
|
ENST00000639739.2:c.*353T>G
(LOX)
|
ENSP00000492324.2:n.*353T>G
|
|
ENST00000231004.4:c.1161T>G
(LOX)
|
ENSP00000231004.4:p.Pro387=
|
|
ENST00000503759.5:n.752T>G
(LOX)
|
|
|
ENST00000504881.1:n.312-5176A>C
(SRFBP1)
|
|
|
ENST00000505593.5:n.487T>G
(LOX)
|
|
|
ENST00000513319.5:n.504T>G
(LOX)
|
|
|
NM_001178102.1:c.471T>G
(LOX)
|
NP_001171573.1:p.Pro157=
|
|
NM_001178102.2:c.471T>G
(LOX)
|
NP_001171573.1:p.Pro157=
|
|
NM_001317073.1:c.270T>G
(LOX)
|
NP_001304002.1:p.Pro90=
|
|
NM_002317.5:c.1161T>G
(LOX)
|
NP_002308.2:p.Pro387=
|
|
NM_002317.6:c.1161T>G
(LOX)
|
NP_002308.2:p.Pro387=
|
|
XM_017009111.2:c.1106-5176A>C
(SRFBP1)
|
XP_016864600.2:n.1106-5176A>C
|
|
NM_002317.7:c.1161T>G
(LOX)
MANE Select
|
NP_002308.2:p.Pro387=
|
|