ENST00000335670.11:c.230G>T
(RORA)
MANE Select
|
ENSP00000335087.6:p.Gly77Val
|
|
ENST00000261523.9:c.329G>T
(RORA)
|
ENSP00000261523.5:p.Gly110Val
|
|
ENST00000309157.8:c.305G>T
(RORA)
|
ENSP00000309753.3:p.Gly102Val
|
|
ENST00000335670.10:c.230G>T
(RORA)
|
ENSP00000335087.6:p.Gly77Val
|
|
ENST00000449337.6:c.65G>T
(RORA)
|
ENSP00000402971.2:p.Gly22Val
|
|
ENST00000551975.5:c.227G>T
(RORA)
|
|
|
ENST00000557822.5:n.255G>T
(RORA)
|
|
|
ENST00000558234.1:n.165G>T
(RORA)
|
|
|
ENST00000559343.1:c.236G>T
(RORA)
|
ENSP00000453322.1:p.Gly79Val
|
|
ENST00000560004.5:n.185G>T
(RORA)
|
|
|
NM_002943.3:c.305G>T
(RORA)
|
NP_002934.1:p.Gly102Val
|
|
NM_134260.2:c.329G>T
(RORA)
|
NP_599022.1:p.Gly110Val
|
|
NM_134261.2:c.230G>T
(RORA)
|
NP_599023.1:p.Gly77Val
|
|
NM_134262.2:c.65G>T
(RORA)
|
NP_599024.1:p.Gly22Val
|
|
NR_120341.1:n.347+21285C>A
(RORA-AS1)
|
|
|
NR_120342.1:n.415+21285C>A
(RORA-AS1)
|
|
|
XM_005254584.3:c.92G>T
(RORA)
|
XP_005254641.1:p.Gly31Val
|
|
XM_011521873.1:c.239G>T
(RORA)
|
XP_011520175.1:p.Gly80Val
|
|
XM_011521874.1:c.236G>T
(RORA)
|
XP_011520176.1:p.Gly79Val
|
|
XM_011521875.1:c.173G>T
(RORA)
|
XP_011520177.1:p.Gly58Val
|
|
XM_011521876.1:c.98G>T
(RORA)
|
XP_011520178.1:p.Gly33Val
|
|
XM_011521877.1:c.62G>T
(RORA)
|
XP_011520179.1:p.Gly21Val
|
|
XM_011521878.1:c.-182G>T
(RORA)
|
XP_011520180.1:n.-182G>T
|
|
XM_005254584.5:c.92G>T
(RORA)
|
XP_005254641.1:p.Gly31Val
|
|
XM_011521875.2:c.173G>T
(RORA)
|
XP_011520177.1:p.Gly58Val
|
|
XM_011521877.3:c.62G>T
(RORA)
|
XP_011520179.1:p.Gly21Val
|
|
XM_011521878.2:c.-182G>T
(RORA)
|
XP_011520180.1:n.-182G>T
|
|
XM_017022466.2:c.41G>T
(RORA)
|
XP_016877955.1:p.Gly14Val
|
|
XM_017022467.2:c.-182G>T
(RORA)
|
XP_016877956.1:n.-182G>T
|
|
NM_134261.3:c.230G>T
(RORA)
MANE Select
|
NP_599023.1:p.Gly77Val
|
|
NM_134262.3:c.65G>T
(RORA)
|
NP_599024.1:p.Gly22Val
|
|
NM_002943.4:c.305G>T
(RORA)
|
NP_002934.1:p.Gly102Val
|
|
NM_134260.3:c.329G>T
(RORA)
|
NP_599022.1:p.Gly110Val
|
|