ENST00000285021.12:c.2169G>C
MANE Select
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ENSP00000285021.8:p.Gln723His
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ENST00000285021.11:c.2169G>C
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ENSP00000285021.7:p.Gln723His
|
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ENST00000427795.2:n.34G>C
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|
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ENST00000476581.6:c.*1622G>C
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ENSP00000424548.1:n.*1622G>C
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NM_004628.4:c.2169G>C , LRG_472t1:c.2169G>C
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NP_004619.3:p.Gln723His
|
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NR_027299.1:n.2149G>C
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|
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XM_011534092.1:c.2169G>C
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XP_011532394.1:p.Gln723His
|
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NM_001354726.1:c.1590G>C
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NP_001341655.1:p.Gln530His
|
|
NM_001354727.1:c.2163G>C
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NP_001341656.1:p.Gln721His
|
|
NM_001354729.1:c.2151G>C
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NP_001341658.1:p.Gln717His
|
|
NM_001354730.1:c.1923G>C
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NP_001341659.1:p.Gln641His
|
|
NR_148950.1:n.2112G>C
|
|
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NR_148951.1:n.1988G>C
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|
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XR_001740256.2:n.2202G>C
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|
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XR_002959580.1:n.2202G>C
|
|
|
XR_002959581.1:n.3819G>C
|
|
|
NM_001354727.2:c.2163G>C
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NP_001341656.1:p.Gln721His
|
|
NM_004628.5:c.2169G>C
MANE Select
|
NP_004619.3:p.Gln723His
|
|
NR_148950.2:n.2041G>C
|
|
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NR_148951.2:n.1917G>C
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|
|
NM_001354726.2:c.1590G>C
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NP_001341655.1:p.Gln530His
|
|
NM_001354729.2:c.2151G>C
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NP_001341658.1:p.Gln717His
|
|
NM_001354730.2:c.1923G>C
|
NP_001341659.1:p.Gln641His
|
|