ENST00000371084.8:c.1166A>C
MANE Select
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ENSP00000360125.3:p.Lys389Thr
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ENST00000650546.1:c.1166A>C
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ENSP00000497812.1:p.Lys389Thr
|
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ENST00000371083.4:c.1220A>C
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ENSP00000360124.4:p.Lys407Thr
|
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ENST00000371084.7:c.1166A>C
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ENSP00000360125.3:p.Lys389Thr
|
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ENST00000540265.5:c.575A>C
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ENSP00000443449.1:p.Lys192Thr
|
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NM_001172818.1:c.1220A>C
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NP_001166289.1:p.Lys407Thr
|
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NM_001172819.1:c.575A>C
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NP_001166290.1:p.Lys192Thr
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NM_002633.2:c.1166A>C
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NP_002624.2:p.Lys389Thr
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NM_002633.3:c.1166A>C
MANE Select
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NP_002624.2:p.Lys389Thr
|
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NM_001172819.2:c.575A>C
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NP_001166290.1:p.Lys192Thr
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