ENST00000304895.9:c.1879T>A
MANE Select
|
ENSP00000302728.4:p.Trp627Arg
|
|
ENST00000304895.8:c.1879T>A
|
ENSP00000302728.4:p.Trp627Arg
|
|
ENST00000421103.5:c.1441T>A
|
ENSP00000391390.1:p.Trp481Arg
|
|
ENST00000430730.5:c.*1146T>A
|
ENSP00000411859.1:n.*1146T>A
|
|
ENST00000447929.5:c.*1259T>A
|
ENSP00000411262.1:n.*1259T>A
|
|
ENST00000466883.5:n.2269T>A
|
|
|
NM_000181.3:c.1879T>A
|
NP_000172.2:p.Trp627Arg
|
|
NM_001284290.1:c.1441T>A
|
NP_001271219.1:p.Trp481Arg
|
|
NM_001293104.1:c.1309T>A
|
NP_001280033.1:p.Trp437Arg
|
|
NM_001293105.1:c.1222T>A
|
NP_001280034.1:p.Trp408Arg
|
|
NR_120531.1:n.1925T>A
|
|
|
XM_005250297.3:c.1726T>A
|
XP_005250354.1:p.Trp576Arg
|
|
XM_011516113.1:c.1378T>A
|
XP_011514415.1:p.Trp460Arg
|
|
XM_011516114.1:c.1207T>A
|
XP_011514416.1:p.Trp403Arg
|
|
XM_005250297.4:c.1726T>A
|
XP_005250354.1:p.Trp576Arg
|
|
XM_011516114.2:c.1207T>A
|
XP_011514416.1:p.Trp403Arg
|
|
XM_017012091.1:c.1225T>A
|
XP_016867580.1:p.Trp409Arg
|
|
XM_017012092.1:c.1156T>A
|
XP_016867581.1:p.Trp386Arg
|
|
XM_017012093.2:c.1054T>A
|
XP_016867582.1:p.Trp352Arg
|
|
XR_001744658.2:n.1686T>A
|
|
|
XR_001744659.2:n.1799T>A
|
|
|
XR_001744660.2:n.1731T>A
|
|
|
XR_001744661.2:n.1646T>A
|
|
|
XR_927461.3:n.1884T>A
|
|
|
NM_000181.4:c.1879T>A
MANE Select
|
NP_000172.2:p.Trp627Arg
|
|
NM_001284290.2:c.1441T>A
|
NP_001271219.1:p.Trp481Arg
|
|
NM_001293104.2:c.1309T>A
|
NP_001280033.1:p.Trp437Arg
|
|
NM_001293105.2:c.1222T>A
|
NP_001280034.1:p.Trp408Arg
|
|
NR_120531.2:n.1824T>A
|
|
|