|
ENST00000361337.3:c.1815G>T
(TOP1)
MANE Select
|
ENSP00000354522.2:p.Leu605=
|
|
|
ENST00000680945.1:c.408G>T
(TOP1)
|
ENSP00000504935.1:p.Leu136=
|
|
|
ENST00000681058.1:n.6601G>T
(TOP1)
|
|
|
|
ENST00000681113.1:c.*1510G>T
(TOP1)
|
ENSP00000505788.1:n.*1510G>T
|
|
|
ENST00000681392.1:n.3123G>T
(TOP1)
|
|
|
|
ENST00000681884.1:n.3077G>T
(TOP1)
|
|
|
|
ENST00000361337.2:c.1815G>T
(TOP1)
|
ENSP00000354522.2:p.Leu605=
|
|
|
NM_003286.2:c.1815G>T
(TOP1)
|
NP_003277.1:p.Leu605=
|
|
|
NR_109889.1:n.711-15096C>A
(PLCG1-AS1)
|
|
|
|
XM_011529032.1:c.1311G>T
(TOP1)
|
XP_011527334.1:p.Leu437=
|
|
|
XM_011529033.1:c.1077G>T
(TOP1)
|
XP_011527335.1:p.Leu359=
|
|
|
NM_003286.3:c.1815G>T
(TOP1)
|
NP_003277.1:p.Leu605=
|
|
|
NM_003286.4:c.1815G>T
(TOP1)
MANE Select
|
NP_003277.1:p.Leu605=
|
|
