ENST00000304895.9:c.1649A>G
MANE Select
|
ENSP00000302728.4:p.His550Arg
|
|
ENST00000304895.8:c.1649A>G
|
ENSP00000302728.4:p.His550Arg
|
|
ENST00000421103.5:c.1211A>G
|
ENSP00000391390.1:p.His404Arg
|
|
ENST00000430730.5:c.*916A>G
|
ENSP00000411859.1:n.*916A>G
|
|
ENST00000447929.5:c.*1029A>G
|
ENSP00000411262.1:n.*1029A>G
|
|
ENST00000461622.1:n.174A>G
|
|
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ENST00000462371.1:n.687A>G
|
|
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ENST00000466883.5:n.2039A>G
|
|
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NM_000181.3:c.1649A>G
|
NP_000172.2:p.His550Arg
|
|
NM_001284290.1:c.1211A>G
|
NP_001271219.1:p.His404Arg
|
|
NM_001293104.1:c.1079A>G
|
NP_001280033.1:p.His360Arg
|
|
NM_001293105.1:c.992A>G
|
NP_001280034.1:p.His331Arg
|
|
NR_120531.1:n.1695A>G
|
|
|
XM_005250297.3:c.1496A>G
|
XP_005250354.1:p.His499Arg
|
|
XM_011516113.1:c.1148A>G
|
XP_011514415.1:p.His383Arg
|
|
XM_011516114.1:c.977A>G
|
XP_011514416.1:p.His326Arg
|
|
XR_927461.1:n.1735A>G
|
|
|
XM_005250297.4:c.1496A>G
|
XP_005250354.1:p.His499Arg
|
|
XM_011516114.2:c.977A>G
|
XP_011514416.1:p.His326Arg
|
|
XM_017012091.1:c.995A>G
|
XP_016867580.1:p.His332Arg
|
|
XM_017012092.1:c.926A>G
|
XP_016867581.1:p.His309Arg
|
|
XM_017012093.2:c.824A>G
|
XP_016867582.1:p.His275Arg
|
|
XR_001744658.2:n.1456A>G
|
|
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XR_001744659.2:n.1569A>G
|
|
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XR_001744660.2:n.1501A>G
|
|
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XR_001744661.2:n.1416A>G
|
|
|
XR_927461.3:n.1654A>G
|
|
|
NM_000181.4:c.1649A>G
MANE Select
|
NP_000172.2:p.His550Arg
|
|
NM_001284290.2:c.1211A>G
|
NP_001271219.1:p.His404Arg
|
|
NM_001293104.2:c.1079A>G
|
NP_001280033.1:p.His360Arg
|
|
NM_001293105.2:c.992A>G
|
NP_001280034.1:p.His331Arg
|
|
NR_120531.2:n.1594A>G
|
|
|