ENST00000269980.7:c.1188G>A
MANE Select
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ENSP00000269980.2:p.Gln396=
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ENST00000269980.6:c.1188G>A
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ENSP00000269980.2:p.Gln396=
|
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ENST00000457836.6:c.1197G>A
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ENSP00000416000.2:p.Gln399=
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ENST00000540732.3:c.1290G>A
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ENSP00000443246.1:p.Gln430=
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ENST00000544905.1:c.62-44G>A
|
|
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ENST00000595085.5:c.922+1761G>A
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ENSP00000471150.2:n.922+1761G>A
|
|
NM_000709.3:c.1188G>A
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NP_000700.1:p.Gln396=
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NM_001164783.1:c.1185G>A
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NP_001158255.1:p.Gln395=
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NM_000709.4:c.1188G>A
MANE Select
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NP_000700.1:p.Gln396=
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NM_001164783.2:c.1185G>A
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NP_001158255.1:p.Gln395=
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