ENST00000361337.3:c.1758C>A
(TOP1)
MANE Select
|
ENSP00000354522.2:p.Ala586=
|
|
ENST00000680945.1:c.351C>A
(TOP1)
|
ENSP00000504935.1:p.Ala117=
|
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ENST00000681058.1:n.6544C>A
(TOP1)
|
|
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ENST00000681113.1:c.*1453C>A
(TOP1)
|
ENSP00000505788.1:n.*1453C>A
|
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ENST00000681392.1:n.3066C>A
(TOP1)
|
|
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ENST00000681884.1:n.3020C>A
(TOP1)
|
|
|
ENST00000361337.2:c.1758C>A
(TOP1)
|
ENSP00000354522.2:p.Ala586=
|
|
NM_003286.2:c.1758C>A
(TOP1)
|
NP_003277.1:p.Ala586=
|
|
NR_109889.1:n.711-15039G>T
(PLCG1-AS1)
|
|
|
XM_011529032.1:c.1254C>A
(TOP1)
|
XP_011527334.1:p.Ala418=
|
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XM_011529033.1:c.1020C>A
(TOP1)
|
XP_011527335.1:p.Ala340=
|
|
NM_003286.3:c.1758C>A
(TOP1)
|
NP_003277.1:p.Ala586=
|
|
NM_003286.4:c.1758C>A
(TOP1)
MANE Select
|
NP_003277.1:p.Ala586=
|
|