ENST00000269980.7:c.810C>T
MANE Select
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ENSP00000269980.2:p.Ala270=
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ENST00000269980.6:c.810C>T
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ENSP00000269980.2:p.Ala270=
|
|
ENST00000457836.6:c.744C>T
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ENSP00000416000.2:p.Ala248=
|
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ENST00000535632.5:n.439C>T
|
|
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ENST00000540732.3:c.912C>T
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ENSP00000443246.1:p.Ala304=
|
|
ENST00000542943.5:c.723C>T
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ENSP00000440345.1:p.Ala241=
|
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ENST00000545787.1:n.438C>T
|
|
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ENST00000595085.5:c.810C>T
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ENSP00000471150.2:p.Ala270=
|
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NM_000709.3:c.810C>T
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NP_000700.1:p.Ala270=
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NM_001164783.1:c.810C>T
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NP_001158255.1:p.Ala270=
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|
NM_000709.4:c.810C>T
MANE Select
|
NP_000700.1:p.Ala270=
|
|
NM_001164783.2:c.810C>T
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NP_001158255.1:p.Ala270=
|
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