ENST00000312465.12:c.642T>A
MANE Select
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ENSP00000311697.7:p.His214Gln
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ENST00000312465.11:c.642T>A
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ENSP00000311697.7:p.His214Gln
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ENST00000456523.3:c.*166T>A
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ENSP00000398353.3:n.*166T>A
|
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ENST00000503413.1:n.591T>A
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|
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ENST00000507780.1:c.342+11495T>A
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ENSP00000423903.1:n.342+11495T>A
|
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NM_001291812.1:c.213T>A
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NP_001278741.1:p.His71Gln
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NM_004464.3:c.642T>A
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NP_004455.2:p.His214Gln
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NM_033143.2:c.*166T>A
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NP_149134.1:n.*166T>A
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NM_001291812.2:c.213T>A
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NP_001278741.1:p.His71Gln
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NM_004464.4:c.642T>A
MANE Select
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NP_004455.2:p.His214Gln
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