ENST00000644719.2:c.606G>A
MANE Select
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ENSP00000496625.1:p.Trp202Ter
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ENST00000418967.6:c.606G>A
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ENSP00000408860.2:p.Trp202Ter
|
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ENST00000435122.3:c.516G>A
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ENSP00000415043.2:p.Trp172Ter
|
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ENST00000462278.1:n.194G>A
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|
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ENST00000464325.5:n.527G>A
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|
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ENST00000466779.5:c.*298G>A
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ENSP00000417321.1:n.*298G>A
|
|
ENST00000466879.5:n.657G>A
|
|
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ENST00000469053.5:c.*298G>A
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ENSP00000418104.1:n.*298G>A
|
|
ENST00000471671.4:c.567G>A
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ENSP00000418561.1:p.Trp189Ter
|
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ENST00000479074.5:n.664G>A
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|
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ENST00000479730.5:n.722G>A
|
|
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ENST00000483041.5:n.775G>A
|
|
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ENST00000486063.5:n.786G>A
|
|
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NM_000500.7:c.606G>A
|
NP_000491.4:p.Trp202Ter
|
|
NM_001128590.3:c.516G>A
|
NP_001122062.3:p.Trp172Ter
|
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XM_011514314.1:c.201G>A
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XP_011512616.1:p.Trp67Ter
|
|
NM_000500.9:c.606G>A
MANE Select
|
NP_000491.4:p.Trp202Ter
|
|
NM_001368143.1:c.201G>A
|
NP_001355072.1:p.Trp67Ter
|
|
NM_001368144.1:c.201G>A
|
NP_001355073.1:p.Trp67Ter
|
|
NM_001128590.4:c.516G>A
|
NP_001122062.3:p.Trp172Ter
|
|
NM_001368143.2:c.201G>A
|
NP_001355072.1:p.Trp67Ter
|
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NM_001368144.2:c.201G>A
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NP_001355073.1:p.Trp67Ter
|
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