ENST00000695651.1:n.2584T>G
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|
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ENST00000695653.1:c.2145T>G
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ENSP00000512084.1:p.Ala715=
|
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ENST00000695654.1:c.3261T>G
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ENSP00000512085.1:p.Ala1087=
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ENST00000695689.1:c.207T>G
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ENSP00000512101.1:n.207T>G
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ENST00000695690.1:n.427T>G
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ENST00000695691.1:n.427T>G
|
|
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ENST00000245907.11:c.4236T>G
MANE Select
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ENSP00000245907.4:p.Ala1412=
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ENST00000245907.10:c.4236T>G
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ENSP00000245907.4:p.Ala1412=
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ENST00000596548.1:c.357T>G
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ENSP00000469744.1:p.Ala119=
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ENST00000599899.5:n.1195T>G
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|
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ENST00000601008.1:c.242-4208T>G
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ENSP00000471384.1:n.242-4208T>G
|
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NM_000064.3:c.4236T>G
|
NP_000055.2:p.Ala1412=
|
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NM_000064.4:c.4236T>G
MANE Select
|
NP_000055.2:p.Ala1412=
|
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