ENST00000644719.2:c.1146C>T
MANE Select
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ENSP00000496625.1:p.Gly382=
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ENST00000418967.6:c.1146C>T
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ENSP00000408860.2:p.Gly382=
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ENST00000435122.3:c.1056C>T
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ENSP00000415043.2:p.Gly352=
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ENST00000479074.5:n.1287C>T
|
|
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ENST00000479730.5:n.1262C>T
|
|
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ENST00000483041.5:n.1315C>T
|
|
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ENST00000486063.5:n.1125C>T
|
|
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NM_000500.7:c.1146C>T
|
NP_000491.4:p.Gly382=
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NM_001128590.3:c.1056C>T
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NP_001122062.3:p.Gly352=
|
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XM_011514314.1:c.741C>T
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XP_011512616.1:p.Gly247=
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NM_000500.9:c.1146C>T
MANE Select
|
NP_000491.4:p.Gly382=
|
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NM_001368143.1:c.741C>T
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NP_001355072.1:p.Gly247=
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NM_001368144.1:c.741C>T
|
NP_001355073.1:p.Gly247=
|
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NM_001128590.4:c.1056C>T
|
NP_001122062.3:p.Gly352=
|
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NM_001368143.2:c.741C>T
|
NP_001355072.1:p.Gly247=
|
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NM_001368144.2:c.741C>T
|
NP_001355073.1:p.Gly247=
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