ENST00000269980.7:c.666A>T
MANE Select
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ENSP00000269980.2:p.Ala222=
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ENST00000269980.6:c.666A>T
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ENSP00000269980.2:p.Ala222=
|
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ENST00000457836.6:c.600A>T
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ENSP00000416000.2:p.Ala200=
|
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ENST00000535632.5:n.295A>T
|
|
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ENST00000538423.5:n.792A>T
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|
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ENST00000540732.3:c.768A>T
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ENSP00000443246.1:p.Ala256=
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ENST00000541315.1:c.566A>T
|
|
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ENST00000542943.5:c.579A>T
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ENSP00000440345.1:p.Ala193=
|
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ENST00000545787.1:n.294A>T
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|
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ENST00000595085.5:c.666A>T
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ENSP00000471150.2:p.Ala222=
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NM_000709.3:c.666A>T
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NP_000700.1:p.Ala222=
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NM_001164783.1:c.666A>T
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NP_001158255.1:p.Ala222=
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NM_000709.4:c.666A>T
MANE Select
|
NP_000700.1:p.Ala222=
|
|
NM_001164783.2:c.666A>T
|
NP_001158255.1:p.Ala222=
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