ENST00000233575.7:c.693T>A
MANE Select
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ENSP00000233575.2:p.Asp231Glu
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ENST00000233575.6:c.693T>A
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ENSP00000233575.2:p.Asp231Glu
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ENST00000427123.5:c.*503T>A
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ENSP00000405399.1:n.*503T>A
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ENST00000440760.5:c.*538T>A
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ENSP00000399727.1:n.*538T>A
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ENST00000453453.1:c.*220T>A
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ENSP00000401922.1:n.*220T>A
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ENST00000493711.1:n.410T>A
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ENST00000494893.5:n.869T>A
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ENST00000537606.5:c.618T>A
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ENSP00000439208.1:p.Asp206Glu
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NM_001267059.1:c.657T>A
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NP_001253988.1:p.Asp219Glu
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NM_001267060.1:c.618T>A
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NP_001253989.1:p.Asp206Glu
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NM_001267061.1:c.633T>A
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NP_001253990.1:p.Asp211Glu
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NM_014748.3:c.693T>A
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NP_055563.1:p.Asp231Glu
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NR_049782.1:n.1066T>A
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NR_049783.1:n.1039T>A
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NR_049784.1:n.1015T>A
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NR_049785.1:n.948T>A
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NR_049786.1:n.897T>A
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NR_049787.1:n.748T>A
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NR_049788.1:n.678T>A
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XM_011533203.1:c.51T>A
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XP_011531505.1:p.Asp17Glu
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XM_011533203.2:c.51T>A
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XP_011531505.1:p.Asp17Glu
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XM_017005405.2:c.51T>A
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XP_016860894.1:p.Asp17Glu
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NM_014748.4:c.693T>A
MANE Select
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NP_055563.1:p.Asp231Glu
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NM_001267059.2:c.657T>A
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NP_001253988.1:p.Asp219Glu
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NM_001267061.2:c.633T>A
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NP_001253990.1:p.Asp211Glu
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NR_049782.2:n.946T>A
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NR_049783.2:n.919T>A
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NR_049784.2:n.895T>A
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NR_049785.2:n.828T>A
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NR_049786.2:n.777T>A
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NR_049787.2:n.628T>A
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NR_049788.2:n.558T>A
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NM_001267060.2:c.618T>A
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NP_001253989.1:p.Asp206Glu
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