ENST00000296684.10:c.354T>G
MANE Select
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ENSP00000296684.5:p.Ala118=
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ENST00000296684.9:c.354T>G
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ENSP00000296684.5:p.Ala118=
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ENST00000502423.5:c.*221T>G
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ENSP00000422177.1:n.*221T>G
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ENST00000506765.1:c.338+12149T>G
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ENSP00000424570.1:n.338+12149T>G
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ENST00000506974.5:c.*130T>G
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ENSP00000425967.1:n.*130T>G
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ENST00000507026.5:c.*328T>G
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ENSP00000424993.1:n.*328T>G
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ENST00000509443.1:n.215T>G
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NM_002495.2:c.354T>G
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NP_002486.1:p.Ala118=
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XM_005248525.3:c.350+12149T>G
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XP_005248582.1:n.350+12149T>G
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XM_011543415.1:c.180T>G
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XP_011541717.1:p.Ala60=
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NM_001318051.1:c.350+12149T>G
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NP_001304980.1:n.350+12149T>G
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NM_002495.3:c.354T>G
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NP_002486.1:p.Ala118=
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NR_134473.1:n.556T>G
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NR_134474.1:n.473T>G
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NR_134475.1:n.508T>G
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NM_002495.4:c.354T>G
MANE Select
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NP_002486.1:p.Ala118=
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NM_001318051.2:c.350+12149T>G
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NP_001304980.1:n.350+12149T>G
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NR_134473.2:n.550T>G
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NR_134474.2:n.467T>G
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NR_134475.2:n.502T>G
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