ENST00000361669.7:c.879C>T
MANE Select
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ENSP00000355316.2:p.Ala293=
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ENST00000361669.6:c.879C>T
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ENSP00000355316.2:p.Ala293=
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ENST00000439827.1:c.879C>T
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ENSP00000398767.1:p.Ala293=
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ENST00000454217.1:c.495C>T
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ENSP00000405427.1:p.Ala165=
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NM_000840.2:c.879C>T
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NP_000831.2:p.Ala293=
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XM_011516088.1:c.879C>T
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XP_011514390.1:p.Ala293=
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XM_011516089.1:c.879C>T
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XP_011514391.1:p.Ala293=
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XM_011516090.1:c.879C>T
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XP_011514392.1:p.Ala293=
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XR_927721.1:n.1425+6516G>A
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NM_001363522.1:c.879C>T
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NP_001350451.1:p.Ala293=
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XM_017012073.2:c.879C>T
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XP_016867562.1:p.Ala293=
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XR_002956570.1:n.90+6516G>A
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XR_002956571.1:n.88+7949G>A
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NM_000840.3:c.879C>T
MANE Select
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NP_000831.2:p.Ala293=
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NM_001363522.2:c.879C>T
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NP_001350451.1:p.Ala293=
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