ENST00000315491.12:c.987G>T
MANE Select
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ENSP00000320295.7:p.Gln329His
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ENST00000680788.1:n.4408G>T
|
|
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ENST00000315491.11:c.987G>T
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ENSP00000320295.7:p.Gln329His
|
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ENST00000554444.5:c.771G>T
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ENSP00000451617.1:p.Gln257His
|
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ENST00000555576.5:c.277+1860G>T
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ENSP00000452554.1:n.277+1860G>T
|
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ENST00000555609.5:c.*1072G>T
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ENSP00000451276.1:n.*1072G>T
|
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ENST00000556922.1:c.2028G>T
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ENSP00000451560.1:p.Gln676His
|
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NM_001197181.1:c.771G>T
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NP_001184110.1:p.Gln257His
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NM_006086.3:c.987G>T
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NP_006077.2:p.Gln329His
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NM_006086.4:c.987G>T
MANE Select
|
NP_006077.2:p.Gln329His
|
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NM_001197181.2:c.771G>T
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NP_001184110.1:p.Gln257His
|
|