ENST00000356839.10:c.641T>G
MANE Select
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ENSP00000349297.5:p.Phe214Cys
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ENST00000322910.9:c.*596T>G
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ENSP00000325395.5:n.*596T>G
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ENST00000350303.9:c.575T>G
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ENSP00000344152.5:p.Phe192Cys
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ENST00000356839.9:c.641T>G
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ENSP00000349297.5:p.Phe214Cys
|
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ENST00000543245.6:c.710T>G
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ENSP00000438689.2:p.Phe237Cys
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ENST00000577191.5:n.718T>G
|
|
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ENST00000577857.5:n.457T>G
|
|
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ENST00000579286.5:n.822T>G
|
|
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ENST00000580365.1:n.372T>G
|
|
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ENST00000581378.5:c.359T>G
|
|
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ENST00000581562.5:n.543T>G
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|
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ENST00000582379.1:n.25T>G
|
|
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ENST00000583312.5:c.656T>G
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ENSP00000467920.1:p.Phe219Cys
|
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ENST00000583760.1:n.423T>G
|
|
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NM_000018.3:c.641T>G
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NP_000009.1:p.Phe214Cys
|
|
NM_001033859.2:c.575T>G
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NP_001029031.1:p.Phe192Cys
|
|
NM_001270447.1:c.710T>G
|
NP_001257376.1:p.Phe237Cys
|
|
NM_001270448.1:c.413T>G
|
NP_001257377.1:p.Phe138Cys
|
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XM_006721516.2:c.641T>G
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XP_006721579.2:p.Phe214Cys
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XM_011523829.1:c.641T>G
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XP_011522131.1:p.Phe214Cys
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XM_011523830.1:c.641T>G
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XP_011522132.1:p.Phe214Cys
|
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XR_934021.1:n.748T>G
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|
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XR_934022.1:n.748T>G
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|
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XR_934023.1:n.748T>G
|
|
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XM_006721516.3:c.641T>G
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XP_006721579.2:p.Phe214Cys
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|
XM_011523829.2:c.641T>G
|
XP_011522131.1:p.Phe214Cys
|
|
XM_011523830.2:c.641T>G
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XP_011522132.1:p.Phe214Cys
|
|
XM_024450741.1:c.641T>G
|
XP_024306509.1:p.Phe214Cys
|
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XR_934021.2:n.700T>G
|
|
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XR_934022.2:n.700T>G
|
|
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XR_934023.2:n.700T>G
|
|
|
NM_000018.4:c.641T>G
MANE Select
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NP_000009.1:p.Phe214Cys
|
|
NM_001033859.3:c.575T>G
|
NP_001029031.1:p.Phe192Cys
|
|
NM_001270447.2:c.710T>G
|
NP_001257376.1:p.Phe237Cys
|
|
NM_001270448.2:c.413T>G
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NP_001257377.1:p.Phe138Cys
|
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