ENST00000361337.3:c.1782C>A
(TOP1)
MANE Select
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ENSP00000354522.2:p.Ala594=
|
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ENST00000680945.1:c.375C>A
(TOP1)
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ENSP00000504935.1:p.Ala125=
|
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ENST00000681058.1:n.6568C>A
(TOP1)
|
|
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ENST00000681113.1:c.*1477C>A
(TOP1)
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ENSP00000505788.1:n.*1477C>A
|
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ENST00000681392.1:n.3090C>A
(TOP1)
|
|
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ENST00000681884.1:n.3044C>A
(TOP1)
|
|
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ENST00000361337.2:c.1782C>A
(TOP1)
|
ENSP00000354522.2:p.Ala594=
|
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NM_003286.2:c.1782C>A
(TOP1)
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NP_003277.1:p.Ala594=
|
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NR_109889.1:n.711-15063G>T
(PLCG1-AS1)
|
|
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XM_011529032.1:c.1278C>A
(TOP1)
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XP_011527334.1:p.Ala426=
|
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XM_011529033.1:c.1044C>A
(TOP1)
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XP_011527335.1:p.Ala348=
|
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NM_003286.3:c.1782C>A
(TOP1)
|
NP_003277.1:p.Ala594=
|
|
NM_003286.4:c.1782C>A
(TOP1)
MANE Select
|
NP_003277.1:p.Ala594=
|
|