ENST00000644719.2:c.171G>C
MANE Select
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ENSP00000496625.1:p.Gly57=
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ENST00000418967.6:c.171G>C
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ENSP00000408860.2:p.Gly57=
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ENST00000435122.3:c.171G>C
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ENSP00000415043.2:p.Gly57=
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ENST00000464325.5:n.11G>C
|
|
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ENST00000466779.5:c.171G>C
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ENSP00000417321.1:p.Gly57=
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ENST00000469053.5:c.171G>C
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ENSP00000418104.1:p.Gly57=
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ENST00000471671.4:c.171G>C
|
ENSP00000418561.1:p.Gly57=
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ENST00000478281.5:c.171G>C
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ENSP00000419572.1:p.Gly57=
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ENST00000479074.5:n.229G>C
|
|
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ENST00000479730.5:n.229G>C
|
|
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ENST00000480027.1:n.224G>C
|
|
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ENST00000483041.5:n.224G>C
|
|
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ENST00000486063.5:n.254G>C
|
|
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ENST00000488465.1:n.179G>C
|
|
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NM_000500.7:c.171G>C
|
NP_000491.4:p.Gly57=
|
|
NM_001128590.3:c.171G>C
|
NP_001122062.3:p.Gly57=
|
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XM_011514314.1:c.-254G>C
|
XP_011512616.1:n.-254G>C
|
|
NM_000500.9:c.171G>C
MANE Select
|
NP_000491.4:p.Gly57=
|
|
NM_001368143.1:c.-254G>C
|
NP_001355072.1:n.-254G>C
|
|
NM_001368144.1:c.-164G>C
|
NP_001355073.1:n.-164G>C
|
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NM_001128590.4:c.171G>C
|
NP_001122062.3:p.Gly57=
|
|
NM_001368143.2:c.-254G>C
|
NP_001355072.1:n.-254G>C
|
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NM_001368144.2:c.-164G>C
|
NP_001355073.1:n.-164G>C
|
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