ENST00000322344.8:c.991T>G
MANE Select
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ENSP00000323511.2:p.Trp331Gly
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ENST00000322344.7:c.991T>G
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ENSP00000323511.2:p.Trp331Gly
|
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ENST00000593706.3:n.346T>G
|
|
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ENST00000593946.5:c.*918T>G
|
ENSP00000468896.1:n.*918T>G
|
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ENST00000594661.5:n.1492T>G
|
|
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ENST00000596014.5:c.991T>G
|
ENSP00000472300.1:p.Trp331Gly
|
|
ENST00000600573.5:c.937-128T>G
|
ENSP00000469826.1:n.937-128T>G
|
|
ENST00000600910.5:c.991T>G
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ENSP00000473137.1:p.Trp331Gly
|
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ENST00000625216.2:c.169T>G
|
ENSP00000486898.1:p.Trp57Gly
|
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ENST00000627232.2:c.911T>G
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ENSP00000486037.1:n.911T>G
|
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ENST00000627317.1:c.612T>G
|
|
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ENST00000629179.1:n.762T>G
|
|
|
ENST00000631020.2:c.883T>G
|
ENSP00000486707.1:p.Trp295Gly
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NM_007254.3:c.991T>G
|
NP_009185.2:p.Trp331Gly
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NM_007254.4:c.991T>G
MANE Select
|
NP_009185.2:p.Trp331Gly
|
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