ENST00000695651.1:n.2065C>T
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|
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ENST00000695652.1:c.3594C>T
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ENSP00000512083.1:p.Ala1198=
|
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ENST00000695653.1:c.1626C>T
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ENSP00000512084.1:p.Ala542=
|
|
ENST00000695654.1:c.2742C>T
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ENSP00000512085.1:p.Ala914=
|
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ENST00000695655.1:c.2658C>T
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ENSP00000512086.1:n.2658C>T
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ENST00000695692.1:n.3081C>T
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|
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ENST00000245907.11:c.3717C>T
MANE Select
|
ENSP00000245907.4:p.Ala1239=
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|
ENST00000245907.10:c.3717C>T
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ENSP00000245907.4:p.Ala1239=
|
|
ENST00000596238.1:n.160C>T
|
|
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ENST00000601008.1:c.241+529C>T
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ENSP00000471384.1:n.241+529C>T
|
|
NM_000064.3:c.3717C>T
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NP_000055.2:p.Ala1239=
|
|
NM_000064.4:c.3717C>T
MANE Select
|
NP_000055.2:p.Ala1239=
|
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