ENST00000361337.3:c.1731T>A
(TOP1)
MANE Select
|
ENSP00000354522.2:p.Leu577=
|
|
ENST00000680945.1:c.324T>A
(TOP1)
|
ENSP00000504935.1:p.Leu108=
|
|
ENST00000681058.1:n.6517T>A
(TOP1)
|
|
|
ENST00000681113.1:c.*1426T>A
(TOP1)
|
ENSP00000505788.1:n.*1426T>A
|
|
ENST00000681392.1:n.3039T>A
(TOP1)
|
|
|
ENST00000681884.1:n.2993T>A
(TOP1)
|
|
|
ENST00000361337.2:c.1731T>A
(TOP1)
|
ENSP00000354522.2:p.Leu577=
|
|
NM_003286.2:c.1731T>A
(TOP1)
|
NP_003277.1:p.Leu577=
|
|
NR_109889.1:n.711-15012A>T
(PLCG1-AS1)
|
|
|
XM_011529032.1:c.1227T>A
(TOP1)
|
XP_011527334.1:p.Leu409=
|
|
XM_011529033.1:c.993T>A
(TOP1)
|
XP_011527335.1:p.Leu331=
|
|
NM_003286.3:c.1731T>A
(TOP1)
|
NP_003277.1:p.Leu577=
|
|
NM_003286.4:c.1731T>A
(TOP1)
MANE Select
|
NP_003277.1:p.Leu577=
|
|