ENST00000269980.7:c.1242G>T
MANE Select
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ENSP00000269980.2:p.Gln414His
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ENST00000269980.6:c.1242G>T
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ENSP00000269980.2:p.Gln414His
|
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ENST00000457836.6:c.1251G>T
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ENSP00000416000.2:p.Gln417His
|
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ENST00000540732.3:c.1344G>T
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ENSP00000443246.1:p.Gln448His
|
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ENST00000544905.1:c.72G>T
|
|
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ENST00000595085.5:c.922+1815G>T
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ENSP00000471150.2:n.922+1815G>T
|
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NM_000709.3:c.1242G>T
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NP_000700.1:p.Gln414His
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NM_001164783.1:c.1239G>T
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NP_001158255.1:p.Gln413His
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NM_000709.4:c.1242G>T
MANE Select
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NP_000700.1:p.Gln414His
|
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NM_001164783.2:c.1239G>T
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NP_001158255.1:p.Gln413His
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