ENST00000361337.3:c.1736A>G
(TOP1)
MANE Select
|
ENSP00000354522.2:p.Asp579Gly
|
|
ENST00000680945.1:c.329A>G
(TOP1)
|
ENSP00000504935.1:p.Asp110Gly
|
|
ENST00000681058.1:n.6522A>G
(TOP1)
|
|
|
ENST00000681113.1:c.*1431A>G
(TOP1)
|
ENSP00000505788.1:n.*1431A>G
|
|
ENST00000681392.1:n.3044A>G
(TOP1)
|
|
|
ENST00000681884.1:n.2998A>G
(TOP1)
|
|
|
ENST00000361337.2:c.1736A>G
(TOP1)
|
ENSP00000354522.2:p.Asp579Gly
|
|
NM_003286.2:c.1736A>G
(TOP1)
|
NP_003277.1:p.Asp579Gly
|
|
NR_109889.1:n.711-15017T>C
(PLCG1-AS1)
|
|
|
XM_011529032.1:c.1232A>G
(TOP1)
|
XP_011527334.1:p.Asp411Gly
|
|
XM_011529033.1:c.998A>G
(TOP1)
|
XP_011527335.1:p.Asp333Gly
|
|
NM_003286.3:c.1736A>G
(TOP1)
|
NP_003277.1:p.Asp579Gly
|
|
NM_003286.4:c.1736A>G
(TOP1)
MANE Select
|
NP_003277.1:p.Asp579Gly
|
|