ENST00000644719.2:c.589G>A
MANE Select
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ENSP00000496625.1:p.Glu197Lys
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ENST00000418967.6:c.589G>A
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ENSP00000408860.2:p.Glu197Lys
|
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ENST00000435122.3:c.499G>A
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ENSP00000415043.2:p.Glu167Lys
|
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ENST00000462278.1:n.177G>A
|
|
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ENST00000464325.5:n.510G>A
|
|
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ENST00000466779.5:c.*281G>A
|
ENSP00000417321.1:n.*281G>A
|
|
ENST00000466879.5:n.640G>A
|
|
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ENST00000469053.5:c.*281G>A
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ENSP00000418104.1:n.*281G>A
|
|
ENST00000471671.4:c.550G>A
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ENSP00000418561.1:p.Glu184Lys
|
|
ENST00000479074.5:n.647G>A
|
|
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ENST00000479730.5:n.705G>A
|
|
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ENST00000483041.5:n.758G>A
|
|
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ENST00000486063.5:n.769G>A
|
|
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NM_000500.7:c.589G>A
|
NP_000491.4:p.Glu197Lys
|
|
NM_001128590.3:c.499G>A
|
NP_001122062.3:p.Glu167Lys
|
|
XM_011514314.1:c.184G>A
|
XP_011512616.1:p.Glu62Lys
|
|
NM_000500.9:c.589G>A
MANE Select
|
NP_000491.4:p.Glu197Lys
|
|
NM_001368143.1:c.184G>A
|
NP_001355072.1:p.Glu62Lys
|
|
NM_001368144.1:c.184G>A
|
NP_001355073.1:p.Glu62Lys
|
|
NM_001128590.4:c.499G>A
|
NP_001122062.3:p.Glu167Lys
|
|
NM_001368143.2:c.184G>A
|
NP_001355072.1:p.Glu62Lys
|
|
NM_001368144.2:c.184G>A
|
NP_001355073.1:p.Glu62Lys
|
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