ENST00000269980.7:c.855A>T
MANE Select
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ENSP00000269980.2:p.Ala285=
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ENST00000269980.6:c.855A>T
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ENSP00000269980.2:p.Ala285=
|
|
ENST00000457836.6:c.789A>T
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ENSP00000416000.2:p.Ala263=
|
|
ENST00000535632.5:n.484A>T
|
|
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ENST00000540732.3:c.957A>T
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ENSP00000443246.1:p.Ala319=
|
|
ENST00000542943.5:c.768A>T
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ENSP00000440345.1:p.Ala256=
|
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ENST00000545787.1:n.483A>T
|
|
|
ENST00000595085.5:c.855A>T
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ENSP00000471150.2:p.Ala285=
|
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NM_000709.3:c.855A>T
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NP_000700.1:p.Ala285=
|
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NM_001164783.1:c.854-2A>T
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NP_001158255.1:n.854-2A>T
|
|
NM_000709.4:c.855A>T
MANE Select
|
NP_000700.1:p.Ala285=
|
|
NM_001164783.2:c.854-2A>T
|
NP_001158255.1:n.854-2A>T
|
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