ENST00000367590.9:c.347A>G
MANE Select
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ENSP00000356562.4:p.His116Arg
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ENST00000367589.3:c.347A>G
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ENSP00000356561.3:p.His116Arg
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ENST00000367590.8:c.347A>G
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ENSP00000356562.4:p.His116Arg
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NM_001135669.1:c.347A>G
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NP_001129141.1:p.His116Arg
|
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NM_004736.3:c.347A>G
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NP_004727.2:p.His116Arg
|
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NM_001328662.1:c.347A>G
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NP_001315591.1:p.His116Arg
|
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NR_137330.1:n.539A>G
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|
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NM_001135669.2:c.347A>G
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NP_001129141.1:p.His116Arg
|
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NM_001328662.2:c.347A>G
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NP_001315591.1:p.His116Arg
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NM_004736.4:c.347A>G
MANE Select
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NP_004727.2:p.His116Arg
|
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NR_137330.2:n.527A>G
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