ENST00000265517.10:c.791G>T
MANE Select
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ENSP00000265517.5:p.Gly264Val
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ENST00000457717.6:c.791G>T
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ENSP00000400821.1:p.Gly264Val
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ENST00000511045.6:c.542G>T
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ENSP00000427679.2:p.Gly181Val
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ENST00000265517.9:c.791G>T
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ENSP00000265517.5:p.Gly264Val
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ENST00000457717.5:c.791G>T
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ENSP00000400821.1:p.Gly264Val
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ENST00000511045.5:c.872G>T
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ENSP00000427679.1:p.Gly291Val
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ENST00000619629.1:c.791G>T
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ENSP00000482850.1:p.Gly264Val
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NM_000253.3:c.791G>T
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NP_000244.2:p.Gly264Val
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NM_001300785.1:c.872G>T
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NP_001287714.1:p.Gly291Val
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NM_000253.4:c.791G>T
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NP_000244.2:p.Gly264Val
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NM_001300785.2:c.542G>T
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NP_001287714.2:p.Gly181Val
|
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NM_001386140.1:c.791G>T
MANE Select
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NP_001373069.1:p.Gly264Val
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