ENST00000326828.6:c.342G>T
MANE Select
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ENSP00000315602.5:p.Gln114His
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ENST00000326828.5:c.342G>T
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ENSP00000315602.5:p.Gln114His
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ENST00000348639.7:c.342G>T
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ENSP00000267951.4:p.Gln114His
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ENST00000559658.5:c.342G>T
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ENSP00000452896.1:p.Gln114His
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NM_000743.4:c.342G>T
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NP_000734.2:p.Gln114His
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NM_001166694.1:c.342G>T
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NP_001160166.1:p.Gln114His
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NR_046313.1:n.843G>T
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|
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XM_006720382.1:c.141G>T
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XP_006720445.1:p.Gln47His
|
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XM_011521173.1:c.261G>T
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XP_011519475.1:p.Gln87His
|
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XM_006720382.3:c.141G>T
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XP_006720445.1:p.Gln47His
|
|
NM_000743.5:c.342G>T
MANE Select
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NP_000734.2:p.Gln114His
|
|
NM_001166694.2:c.342G>T
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NP_001160166.1:p.Gln114His
|
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NR_046313.2:n.544G>T
|
|
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