ENST00000644719.2:c.527T>G
MANE Select
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ENSP00000496625.1:p.Leu176Arg
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ENST00000418967.6:c.527T>G
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ENSP00000408860.2:p.Leu176Arg
|
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ENST00000435122.3:c.437T>G
|
ENSP00000415043.2:p.Leu146Arg
|
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ENST00000462278.1:n.115T>G
|
|
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ENST00000464325.5:n.448T>G
|
|
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ENST00000466779.5:c.*219T>G
|
ENSP00000417321.1:n.*219T>G
|
|
ENST00000466879.5:n.578T>G
|
|
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ENST00000469053.5:c.*219T>G
|
ENSP00000418104.1:n.*219T>G
|
|
ENST00000471671.4:c.527T>G
|
ENSP00000418561.1:p.Leu176Arg
|
|
ENST00000479074.5:n.585T>G
|
|
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ENST00000479730.5:n.682T>G
|
|
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ENST00000483041.5:n.696T>G
|
|
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ENST00000486063.5:n.707T>G
|
|
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ENST00000488465.1:n.535T>G
|
|
|
NM_000500.7:c.527T>G
|
NP_000491.4:p.Leu176Arg
|
|
NM_001128590.3:c.437T>G
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NP_001122062.3:p.Leu146Arg
|
|
XM_011514314.1:c.122T>G
|
XP_011512616.1:p.Leu41Arg
|
|
NM_000500.9:c.527T>G
MANE Select
|
NP_000491.4:p.Leu176Arg
|
|
NM_001368143.1:c.122T>G
|
NP_001355072.1:p.Leu41Arg
|
|
NM_001368144.1:c.122T>G
|
NP_001355073.1:p.Leu41Arg
|
|
NM_001128590.4:c.437T>G
|
NP_001122062.3:p.Leu146Arg
|
|
NM_001368143.2:c.122T>G
|
NP_001355072.1:p.Leu41Arg
|
|
NM_001368144.2:c.122T>G
|
NP_001355073.1:p.Leu41Arg
|
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