ENST00000322344.8:c.1453C>G
MANE Select
|
ENSP00000323511.2:p.Gln485Glu
|
|
ENST00000636840.1:c.59+247C>G
|
|
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ENST00000640501.1:c.55C>G
|
|
|
ENST00000322344.7:c.1453C>G
|
ENSP00000323511.2:p.Gln485Glu
|
|
ENST00000593946.5:c.*1380C>G
|
ENSP00000468896.1:n.*1380C>G
|
|
ENST00000594661.5:n.1954C>G
|
|
|
ENST00000595081.5:n.356C>G
|
|
|
ENST00000596014.5:c.1453C>G
|
ENSP00000472300.1:p.Gln485Glu
|
|
ENST00000597965.2:c.243C>G
|
ENSP00000471097.2:n.243C>G
|
|
ENST00000599454.5:n.373C>G
|
|
|
ENST00000600573.5:c.1360C>G
|
ENSP00000469826.1:p.Gln454Glu
|
|
ENST00000600910.5:c.1343C>G
|
ENSP00000473137.1:p.Ala448Gly
|
|
ENST00000601816.3:n.525C>G
|
|
|
ENST00000625216.2:c.534C>G
|
ENSP00000486898.1:n.534C>G
|
|
ENST00000627232.2:c.1373C>G
|
ENSP00000486037.1:n.1373C>G
|
|
ENST00000631020.2:c.1345C>G
|
ENSP00000486707.1:p.Gln449Glu
|
|
NM_007254.3:c.1453C>G
|
NP_009185.2:p.Gln485Glu
|
|
NM_007254.4:c.1453C>G
MANE Select
|
NP_009185.2:p.Gln485Glu
|
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