ENST00000644719.2:c.691A>G
MANE Select
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ENSP00000496625.1:p.Ile231Val
|
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ENST00000418967.6:c.691A>G
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ENSP00000408860.2:p.Ile231Val
|
|
ENST00000435122.3:c.601A>G
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ENSP00000415043.2:p.Ile201Val
|
|
ENST00000462278.1:n.380A>G
|
|
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ENST00000466779.5:c.*383A>G
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ENSP00000417321.1:n.*383A>G
|
|
ENST00000466879.5:n.742A>G
|
|
|
ENST00000479074.5:n.749A>G
|
|
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ENST00000479730.5:n.807A>G
|
|
|
ENST00000483041.5:n.860A>G
|
|
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ENST00000486063.5:n.871A>G
|
|
|
NM_000500.7:c.691A>G
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NP_000491.4:p.Ile231Val
|
|
NM_001128590.3:c.601A>G
|
NP_001122062.3:p.Ile201Val
|
|
XM_011514314.1:c.286A>G
|
XP_011512616.1:p.Ile96Val
|
|
NM_000500.9:c.691A>G
MANE Select
|
NP_000491.4:p.Ile231Val
|
|
NM_001368143.1:c.286A>G
|
NP_001355072.1:p.Ile96Val
|
|
NM_001368144.1:c.286A>G
|
NP_001355073.1:p.Ile96Val
|
|
NM_001128590.4:c.601A>G
|
NP_001122062.3:p.Ile201Val
|
|
NM_001368143.2:c.286A>G
|
NP_001355072.1:p.Ile96Val
|
|
NM_001368144.2:c.286A>G
|
NP_001355073.1:p.Ile96Val
|
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