ENST00000557658.6:c.677A>G
MANE Select
|
ENSP00000452191.1:p.His226Arg
|
|
ENST00000327028.8:c.530A>G
|
ENSP00000313098.5:p.His177Arg
|
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ENST00000343765.6:c.677A>G
|
ENSP00000339122.2:p.His226Arg
|
|
ENST00000448935.6:c.530A>G
|
ENSP00000404815.2:p.His177Arg
|
|
ENST00000553576.5:n.89A>G
|
|
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ENST00000553691.5:n.567A>G
|
|
|
ENST00000553888.5:c.677A>G
|
ENSP00000452181.1:p.His226Arg
|
|
ENST00000555854.1:n.122A>G
|
|
|
ENST00000556412.4:c.755A>G
|
ENSP00000451857.1:p.His252Arg
|
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ENST00000557658.5:c.677A>G
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ENSP00000452191.1:p.His226Arg
|
|
NM_001193314.1:c.677A>G
|
NP_001180243.1:p.His226Arg
|
|
NM_001193315.1:c.677A>G
|
NP_001180244.1:p.His226Arg
|
|
NM_001193316.1:c.530A>G
|
NP_001180245.1:p.His177Arg
|
|
NM_001193317.1:c.677A>G
|
NP_001180246.1:p.His226Arg
|
|
NM_022067.3:c.677A>G
|
NP_071350.2:p.His226Arg
|
|
XM_011537066.1:c.584A>G
|
XP_011535368.1:p.His195Arg
|
|
XM_011537066.2:c.584A>G
|
XP_011535368.1:p.His195Arg
|
|
XM_017021580.2:c.677A>G
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XP_016877069.1:p.His226Arg
|
|
XM_017021581.2:c.677A>G
|
XP_016877070.1:p.His226Arg
|
|
XM_024449688.1:c.584A>G
|
XP_024305456.1:p.His195Arg
|
|
XR_001750501.2:n.799A>G
|
|
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NM_001193314.2:c.677A>G
|
NP_001180243.1:p.His226Arg
|
|
NM_001193316.2:c.530A>G
|
NP_001180245.1:p.His177Arg
|
|
NM_001193317.2:c.677A>G
|
NP_001180246.1:p.His226Arg
|
|
NM_022067.4:c.677A>G
|
NP_071350.2:p.His226Arg
|
|
NM_001193315.2:c.677A>G
MANE Select
|
NP_001180244.1:p.His226Arg
|
|
NM_001400324.1:c.530A>G
|
NP_001387253.1:p.His177Arg
|
|
NM_001400325.1:c.530A>G
|
NP_001387254.1:p.His177Arg
|
|
NM_001400326.1:c.677A>G
|
NP_001387255.1:p.His226Arg
|
|
NM_001400327.1:c.644A>G
|
NP_001387256.1:p.His215Arg
|
|
NM_001400330.1:c.677A>G
|
NP_001387259.1:p.His226Arg
|
|
NM_001400331.1:c.677A>G
|
NP_001387260.1:p.His226Arg
|
|
NM_001400332.1:c.677A>G
|
NP_001387261.1:p.His226Arg
|
|
NM_001400333.1:c.584A>G
|
NP_001387262.1:p.His195Arg
|
|
NM_001400334.1:c.584A>G
|
NP_001387263.1:p.His195Arg
|
|
NM_001400335.1:c.677A>G
|
NP_001387264.1:p.His226Arg
|
|
NM_001400336.1:c.677A>G
|
NP_001387265.1:p.His226Arg
|
|
NM_001400337.1:c.437A>G
|
NP_001387266.1:p.His146Arg
|
|
NM_001400338.1:c.677A>G
|
NP_001387267.1:p.His226Arg
|
|
NM_001400339.1:c.677A>G
|
NP_001387268.1:p.His226Arg
|
|
NR_174476.1:n.784A>G
|
|
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