|
NM_134261.3:c.1447C>T
(RORA)
MANE Select
|
NP_599023.1:p.Arg483Ter
|
|
ENST00000335670.11:c.1447C>T
(RORA)
MANE Select
|
ENSP00000335087.6:p.Arg483Ter
|
|
NM_002943.3:c.1522C>T
(RORA)
|
NP_002934.1:p.Arg508Ter
|
|
NM_002943.4:c.1522C>T
(RORA)
|
NP_002934.1:p.Arg508Ter
|
|
NM_134260.2:c.1546C>T
(RORA)
|
NP_599022.1:p.Arg516Ter
|
|
NM_134260.3:c.1546C>T
(RORA)
|
NP_599022.1:p.Arg516Ter
|
|
NM_134261.2:c.1447C>T
(RORA)
|
NP_599023.1:p.Arg483Ter
|
|
NM_134262.2:c.1282C>T
(RORA)
|
NP_599024.1:p.Arg428Ter
|
|
NM_134262.3:c.1282C>T
(RORA)
|
NP_599024.1:p.Arg428Ter
|
|
NR_120339.1:n.289+8989G>A
(RORA-AS1)
|
|
|
NR_120340.1:n.289+8989G>A
(RORA-AS1)
|
|
|
NR_120341.1:n.222-12828G>A
(RORA-AS1)
|
|
|
NR_120342.1:n.289+8989G>A
(RORA-AS1)
|
|
|
ENST00000261523.9:c.1546C>T
(RORA)
|
ENSP00000261523.5:p.Arg516Ter
|
|
ENST00000309157.8:c.1522C>T
(RORA)
|
ENSP00000309753.3:p.Arg508Ter
|
|
ENST00000335670.10:c.1447C>T
(RORA)
|
ENSP00000335087.6:p.Arg483Ter
|
|
ENST00000449337.6:c.1282C>T
(RORA)
|
ENSP00000402971.2:p.Arg428Ter
|
|
XM_005254584.3:c.1309C>T
(RORA)
|
XP_005254641.1:p.Arg437Ter
|
|
XM_005254584.5:c.1309C>T
(RORA)
|
XP_005254641.1:p.Arg437Ter
|
|
XM_011521873.1:c.1456C>T
(RORA)
|
XP_011520175.1:p.Arg486Ter
|
|
XM_011521874.1:c.1453C>T
(RORA)
|
XP_011520176.1:p.Arg485Ter
|
|
XM_011521875.1:c.1390C>T
(RORA)
|
XP_011520177.1:p.Arg464Ter
|
|
XM_011521875.2:c.1390C>T
(RORA)
|
XP_011520177.1:p.Arg464Ter
|
|
XM_011521876.1:c.1315C>T
(RORA)
|
XP_011520178.1:p.Arg439Ter
|
|
XM_011521877.1:c.1279C>T
(RORA)
|
XP_011520179.1:p.Arg427Ter
|
|
XM_011521877.3:c.1279C>T
(RORA)
|
XP_011520179.1:p.Arg427Ter
|
|
XM_011521878.1:c.1036C>T
(RORA)
|
XP_011520180.1:p.Arg346Ter
|
|
XM_011521878.2:c.1036C>T
(RORA)
|
XP_011520180.1:p.Arg346Ter
|
|
XM_011521879.1:c.1006C>T
(RORA)
|
XP_011520181.1:p.Arg336Ter
|
|
XM_011521879.3:c.1006C>T
(RORA)
|
XP_011520181.1:p.Arg336Ter
|
|
XM_017022466.2:c.1258C>T
(RORA)
|
XP_016877955.1:p.Arg420Ter
|
|
XM_017022467.2:c.1036C>T
(RORA)
|
XP_016877956.1:p.Arg346Ter
|
