ENST00000361337.3:c.1750T>C
(TOP1)
MANE Select
|
ENSP00000354522.2:p.Leu584=
|
|
ENST00000680945.1:c.343T>C
(TOP1)
|
ENSP00000504935.1:p.Leu115=
|
|
ENST00000681058.1:n.6536T>C
(TOP1)
|
|
|
ENST00000681113.1:c.*1445T>C
(TOP1)
|
ENSP00000505788.1:n.*1445T>C
|
|
ENST00000681392.1:n.3058T>C
(TOP1)
|
|
|
ENST00000681884.1:n.3012T>C
(TOP1)
|
|
|
ENST00000361337.2:c.1750T>C
(TOP1)
|
ENSP00000354522.2:p.Leu584=
|
|
NM_003286.2:c.1750T>C
(TOP1)
|
NP_003277.1:p.Leu584=
|
|
NR_109889.1:n.711-15031A>G
(PLCG1-AS1)
|
|
|
XM_011529032.1:c.1246T>C
(TOP1)
|
XP_011527334.1:p.Leu416=
|
|
XM_011529033.1:c.1012T>C
(TOP1)
|
XP_011527335.1:p.Leu338=
|
|
NM_003286.3:c.1750T>C
(TOP1)
|
NP_003277.1:p.Leu584=
|
|
NM_003286.4:c.1750T>C
(TOP1)
MANE Select
|
NP_003277.1:p.Leu584=
|
|