ENST00000644719.2:c.468C>T
MANE Select
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ENSP00000496625.1:p.Gly156=
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ENST00000418967.6:c.468C>T
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ENSP00000408860.2:p.Gly156=
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ENST00000435122.3:c.378C>T
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ENSP00000415043.2:p.Gly126=
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ENST00000462278.1:n.56C>T
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ENST00000464325.5:n.389C>T
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ENST00000466779.5:c.*160C>T
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ENSP00000417321.1:n.*160C>T
|
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ENST00000466879.5:n.519C>T
|
|
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ENST00000469053.5:c.*160C>T
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ENSP00000418104.1:n.*160C>T
|
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ENST00000471671.4:c.468C>T
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ENSP00000418561.1:p.Gly156=
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ENST00000478281.5:c.501C>T
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ENSP00000419572.1:p.Gly167=
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ENST00000479074.5:n.526C>T
|
|
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ENST00000479730.5:n.623C>T
|
|
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ENST00000483041.5:n.637C>T
|
|
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ENST00000486063.5:n.648C>T
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ENST00000488465.1:n.476C>T
|
|
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NM_000500.7:c.468C>T
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NP_000491.4:p.Gly156=
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NM_001128590.3:c.378C>T
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NP_001122062.3:p.Gly126=
|
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XM_011514314.1:c.63C>T
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XP_011512616.1:p.Gly21=
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NM_000500.9:c.468C>T
MANE Select
|
NP_000491.4:p.Gly156=
|
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NM_001368143.1:c.63C>T
|
NP_001355072.1:p.Gly21=
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|
NM_001368144.1:c.63C>T
|
NP_001355073.1:p.Gly21=
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NM_001128590.4:c.378C>T
|
NP_001122062.3:p.Gly126=
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NM_001368143.2:c.63C>T
|
NP_001355072.1:p.Gly21=
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NM_001368144.2:c.63C>T
|
NP_001355073.1:p.Gly21=
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