ENST00000503581.6:c.7026T>G
MANE Select
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ENSP00000424243.1:p.His2342Gln
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ENST00000370616.6:c.7026T>G
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ENSP00000359650.2:p.His2342Gln
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ENST00000370618.7:c.7026T>G
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ENSP00000359652.4:p.His2342Gln
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ENST00000370621.7:c.7026T>G
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ENSP00000359655.3:p.His2342Gln
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ENST00000398580.3:c.340T>G
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|
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ENST00000503581.5:c.7026T>G
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ENSP00000424243.1:p.His2342Gln
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NM_001142800.1:c.7026T>G
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NP_001136272.1:p.His2342Gln
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NM_001292009.1:c.7026T>G
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NP_001278938.1:p.His2342Gln
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XR_001744188.1:n.606+16128A>C
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XR_001744189.1:n.129+16128A>C
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XR_001744190.1:n.197+16128A>C
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|
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XR_001744191.1:n.607-1242A>C
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|
|
NM_001142800.2:c.7026T>G
MANE Select
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NP_001136272.1:p.His2342Gln
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|
NM_001292009.2:c.7026T>G
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NP_001278938.1:p.His2342Gln
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