ENST00000436068.2:c.*3029C>A
(NCOR1)
|
ENSP00000389839.2:n.*3029C>A
|
|
ENST00000704743.1:n.9300C>A
(NCOR1)
|
|
|
ENST00000704744.1:c.*3029C>A
(NCOR1)
|
ENSP00000516021.1:n.*3029C>A
|
|
ENST00000704745.1:c.*3029C>A
(NCOR1)
|
ENSP00000516022.1:n.*3029C>A
|
|
ENST00000261647.10:c.*1745G>T
(TTC19)
MANE Select
|
ENSP00000261647.5:n.*1745G>T
|
|
ENST00000268712.8:c.*3029C>A
(NCOR1)
MANE Select
|
ENSP00000268712.2:n.*3029C>A
|
|
ENST00000268712.7:c.*3029C>A
(NCOR1)
|
ENSP00000268712.2:n.*3029C>A
|
|
ENST00000470649.1:c.247+2565G>T
(TTC19)
|
ENSP00000465627.1:n.247+2565G>T
|
|
NM_001271420.1:c.*1745G>T
(TTC19)
|
NP_001258349.1:n.*1745G>T
|
|
NM_017775.3:c.*1745G>T
(TTC19)
|
NP_060245.3:n.*1745G>T
|
|
XM_017024801.2:c.994+2565G>T
(TTC19)
|
XP_016880290.2:n.994+2565G>T
|
|
XM_017024802.2:c.994+2565G>T
(TTC19)
|
XP_016880291.2:n.994+2565G>T
|
|
NM_006311.4:c.*3029C>A
(NCOR1)
MANE Select
|
NP_006302.2:n.*3029C>A
|
|
NM_017775.4:c.*1745G>T
(TTC19)
MANE Select
|
NP_060245.3:n.*1745G>T
|
|
NM_001271420.2:c.*1745G>T
(TTC19)
|
NP_001258349.1:n.*1745G>T
|
|