ENST00000304895.9:c.1879T>G
MANE Select
|
ENSP00000302728.4:p.Trp627Gly
|
|
ENST00000304895.8:c.1879T>G
|
ENSP00000302728.4:p.Trp627Gly
|
|
ENST00000421103.5:c.1441T>G
|
ENSP00000391390.1:p.Trp481Gly
|
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ENST00000430730.5:c.*1146T>G
|
ENSP00000411859.1:n.*1146T>G
|
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ENST00000447929.5:c.*1259T>G
|
ENSP00000411262.1:n.*1259T>G
|
|
ENST00000466883.5:n.2269T>G
|
|
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NM_000181.3:c.1879T>G
|
NP_000172.2:p.Trp627Gly
|
|
NM_001284290.1:c.1441T>G
|
NP_001271219.1:p.Trp481Gly
|
|
NM_001293104.1:c.1309T>G
|
NP_001280033.1:p.Trp437Gly
|
|
NM_001293105.1:c.1222T>G
|
NP_001280034.1:p.Trp408Gly
|
|
NR_120531.1:n.1925T>G
|
|
|
XM_005250297.3:c.1726T>G
|
XP_005250354.1:p.Trp576Gly
|
|
XM_011516113.1:c.1378T>G
|
XP_011514415.1:p.Trp460Gly
|
|
XM_011516114.1:c.1207T>G
|
XP_011514416.1:p.Trp403Gly
|
|
XM_005250297.4:c.1726T>G
|
XP_005250354.1:p.Trp576Gly
|
|
XM_011516114.2:c.1207T>G
|
XP_011514416.1:p.Trp403Gly
|
|
XM_017012091.1:c.1225T>G
|
XP_016867580.1:p.Trp409Gly
|
|
XM_017012092.1:c.1156T>G
|
XP_016867581.1:p.Trp386Gly
|
|
XM_017012093.2:c.1054T>G
|
XP_016867582.1:p.Trp352Gly
|
|
XR_001744658.2:n.1686T>G
|
|
|
XR_001744659.2:n.1799T>G
|
|
|
XR_001744660.2:n.1731T>G
|
|
|
XR_001744661.2:n.1646T>G
|
|
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XR_927461.3:n.1884T>G
|
|
|
NM_000181.4:c.1879T>G
MANE Select
|
NP_000172.2:p.Trp627Gly
|
|
NM_001284290.2:c.1441T>G
|
NP_001271219.1:p.Trp481Gly
|
|
NM_001293104.2:c.1309T>G
|
NP_001280033.1:p.Trp437Gly
|
|
NM_001293105.2:c.1222T>G
|
NP_001280034.1:p.Trp408Gly
|
|
NR_120531.2:n.1824T>G
|
|
|