ENST00000644719.2:c.890C>G
MANE Select
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ENSP00000496625.1:p.Thr297Arg
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ENST00000418967.6:c.890C>G
|
ENSP00000408860.2:p.Thr297Arg
|
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ENST00000435122.3:c.800C>G
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ENSP00000415043.2:p.Thr267Arg
|
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ENST00000479074.5:n.948C>G
|
|
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ENST00000479730.5:n.1006C>G
|
|
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ENST00000483041.5:n.1059C>G
|
|
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ENST00000486063.5:n.919-250C>G
|
|
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NM_000500.7:c.890C>G
|
NP_000491.4:p.Thr297Arg
|
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NM_001128590.3:c.800C>G
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NP_001122062.3:p.Thr267Arg
|
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XM_011514314.1:c.485C>G
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XP_011512616.1:p.Thr162Arg
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NM_000500.9:c.890C>G
MANE Select
|
NP_000491.4:p.Thr297Arg
|
|
NM_001368143.1:c.485C>G
|
NP_001355072.1:p.Thr162Arg
|
|
NM_001368144.1:c.485C>G
|
NP_001355073.1:p.Thr162Arg
|
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NM_001128590.4:c.800C>G
|
NP_001122062.3:p.Thr267Arg
|
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NM_001368143.2:c.485C>G
|
NP_001355072.1:p.Thr162Arg
|
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NM_001368144.2:c.485C>G
|
NP_001355073.1:p.Thr162Arg
|
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