ENST00000369244.7:c.1791G>T
MANE Select
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ENSP00000358247.1:p.Gln597His
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ENST00000229971.2:c.1791G>T
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ENSP00000229971.1:p.Gln597His
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ENST00000369244.6:c.1791G>T
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ENSP00000358247.1:p.Gln597His
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NM_001278716.1:c.1791G>T
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NP_001265645.1:p.Gln597His
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NM_012160.4:c.1791G>T
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NP_036292.2:p.Gln597His
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NR_103836.1:n.1836G>T
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XM_005266930.1:c.1719G>T
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XP_005266987.1:p.Gln573His
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XM_005266930.3:c.1719G>T
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XP_005266987.1:p.Gln573His
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XM_017010726.1:c.1791G>T
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XP_016866215.1:p.Gln597His
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XM_017010727.2:c.1719G>T
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XP_016866216.1:p.Gln573His
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XM_017010728.1:c.1065G>T
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XP_016866217.1:p.Gln355His
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NM_001278716.2:c.1791G>T
MANE Select
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NP_001265645.1:p.Gln597His
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NR_103836.2:n.1776G>T
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NM_012160.5:c.1791G>T
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NP_036292.2:p.Gln597His
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