ENST00000296684.10:c.357T>G
MANE Select
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ENSP00000296684.5:p.Asp119Glu
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ENST00000296684.9:c.357T>G
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ENSP00000296684.5:p.Asp119Glu
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ENST00000502423.5:c.*224T>G
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ENSP00000422177.1:n.*224T>G
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ENST00000506765.1:c.338+12152T>G
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ENSP00000424570.1:n.338+12152T>G
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ENST00000506974.5:c.*133T>G
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ENSP00000425967.1:n.*133T>G
|
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ENST00000507026.5:c.*331T>G
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ENSP00000424993.1:n.*331T>G
|
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ENST00000509443.1:n.218T>G
|
|
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NM_002495.2:c.357T>G
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NP_002486.1:p.Asp119Glu
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XM_005248525.3:c.350+12152T>G
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XP_005248582.1:n.350+12152T>G
|
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XM_011543415.1:c.183T>G
|
XP_011541717.1:p.Asp61Glu
|
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NM_001318051.1:c.350+12152T>G
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NP_001304980.1:n.350+12152T>G
|
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NM_002495.3:c.357T>G
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NP_002486.1:p.Asp119Glu
|
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NR_134473.1:n.559T>G
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|
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NR_134474.1:n.476T>G
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|
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NR_134475.1:n.511T>G
|
|
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NM_002495.4:c.357T>G
MANE Select
|
NP_002486.1:p.Asp119Glu
|
|
NM_001318051.2:c.350+12152T>G
|
NP_001304980.1:n.350+12152T>G
|
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NR_134473.2:n.553T>G
|
|
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NR_134474.2:n.470T>G
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NR_134475.2:n.505T>G
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