ENST00000335670.11:c.197-59231G>C
(RORA)
MANE Select
|
ENSP00000335087.6:n.197-59231G>C
|
|
ENST00000261523.9:c.138-32776G>C
(RORA)
|
ENSP00000261523.5:n.138-32776G>C
|
|
ENST00000309157.8:c.271+23812G>C
(RORA)
|
ENSP00000309753.3:n.271+23812G>C
|
|
ENST00000335670.10:c.197-59231G>C
(RORA)
|
ENSP00000335087.6:n.197-59231G>C
|
|
ENST00000449337.6:c.31+1305G>C
(RORA)
|
ENSP00000402971.2:n.31+1305G>C
|
|
ENST00000551975.5:c.194-59231G>C
(RORA)
|
|
|
ENST00000557822.5:n.222-59231G>C
(RORA)
|
|
|
ENST00000558234.1:n.131+1305G>C
(RORA)
|
|
|
ENST00000559343.1:c.202+1726G>C
(RORA)
|
ENSP00000453322.1:n.202+1726G>C
|
|
ENST00000560004.5:n.152-59231G>C
(RORA)
|
|
|
NM_002943.3:c.271+23812G>C
(RORA)
|
NP_002934.1:n.271+23812G>C
|
|
NM_134260.2:c.138-32776G>C
(RORA)
|
NP_599022.1:n.138-32776G>C
|
|
NM_134261.2:c.197-59231G>C
(RORA)
|
NP_599023.1:n.197-59231G>C
|
|
NM_134262.2:c.31+1305G>C
(RORA)
|
NP_599024.1:n.31+1305G>C
|
|
NR_120341.1:n.348-7366C>G
(RORA-AS1)
|
|
|
NR_120342.1:n.416-7366C>G
(RORA-AS1)
|
|
|
XM_005254584.3:c.59-59231G>C
(RORA)
|
XP_005254641.1:n.59-59231G>C
|
|
XM_011521874.1:c.202+1726G>C
(RORA)
|
XP_011520176.1:n.202+1726G>C
|
|
XM_011521875.1:c.140-59231G>C
(RORA)
|
XP_011520177.1:n.140-59231G>C
|
|
XM_011521876.1:c.65-59231G>C
(RORA)
|
XP_011520178.1:n.65-59231G>C
|
|
XM_011521877.1:c.28+2614G>C
(RORA)
|
XP_011520179.1:n.28+2614G>C
|
|
XM_011521878.1:c.-215-59231G>C
(RORA)
|
XP_011520180.1:n.-215-59231G>C
|
|
XM_005254584.5:c.59-59231G>C
(RORA)
|
XP_005254641.1:n.59-59231G>C
|
|
XM_011521875.2:c.140-59231G>C
(RORA)
|
XP_011520177.1:n.140-59231G>C
|
|
XM_011521877.3:c.28+2614G>C
(RORA)
|
XP_011520179.1:n.28+2614G>C
|
|
XM_011521878.2:c.-215-59231G>C
(RORA)
|
XP_011520180.1:n.-215-59231G>C
|
|
XM_017022467.2:c.-216+36156G>C
(RORA)
|
XP_016877956.1:n.-216+36156G>C
|
|
NM_134261.3:c.197-59231G>C
(RORA)
MANE Select
|
NP_599023.1:n.197-59231G>C
|
|
NM_134262.3:c.31+1305G>C
(RORA)
|
NP_599024.1:n.31+1305G>C
|
|
NM_002943.4:c.271+23812G>C
(RORA)
|
NP_002934.1:n.271+23812G>C
|
|
NM_134260.3:c.138-32776G>C
(RORA)
|
NP_599022.1:n.138-32776G>C
|
|