ENST00000361337.3:c.1822+141C>T
(TOP1)
MANE Select
|
ENSP00000354522.2:n.1822+141C>T
|
|
ENST00000680945.1:c.415+141C>T
(TOP1)
|
ENSP00000504935.1:n.415+141C>T
|
|
ENST00000681058.1:n.6608+141C>T
(TOP1)
|
|
|
ENST00000681113.1:c.*1517+141C>T
(TOP1)
|
ENSP00000505788.1:n.*1517+141C>T
|
|
ENST00000681392.1:n.3130+141C>T
(TOP1)
|
|
|
ENST00000681884.1:n.3084+141C>T
(TOP1)
|
|
|
ENST00000361337.2:c.1822+141C>T
(TOP1)
|
ENSP00000354522.2:n.1822+141C>T
|
|
NM_003286.2:c.1822+141C>T
(TOP1)
|
NP_003277.1:n.1822+141C>T
|
|
NR_109889.1:n.711-15244G>A
(PLCG1-AS1)
|
|
|
XM_011529032.1:c.1318+141C>T
(TOP1)
|
XP_011527334.1:n.1318+141C>T
|
|
XM_011529033.1:c.1084+141C>T
(TOP1)
|
XP_011527335.1:n.1084+141C>T
|
|
NM_003286.3:c.1822+141C>T
(TOP1)
|
NP_003277.1:n.1822+141C>T
|
|
NM_003286.4:c.1822+141C>T
(TOP1)
MANE Select
|
NP_003277.1:n.1822+141C>T
|
|