ENST00000261304.7:c.488G>A
MANE Select
|
ENSP00000261304.2:p.Trp163Ter
|
|
ENST00000261304.6:c.488G>A
|
ENSP00000261304.2:p.Trp163Ter
|
|
ENST00000393568.8:c.419G>A
|
ENSP00000377198.4:p.Trp140Ter
|
|
ENST00000393569.6:c.410G>A
|
ENSP00000377199.2:p.Trp137Ter
|
|
ENST00000474294.6:n.478G>A
|
|
|
ENST00000544807.6:c.320G>A
|
ENSP00000437513.2:p.Trp107Ter
|
|
ENST00000554372.5:c.*237G>A
|
ENSP00000451884.1:n.*237G>A
|
|
ENST00000554916.5:n.367G>A
|
|
|
ENST00000556261.5:n.189G>A
|
|
|
ENST00000556879.5:c.548G>A
|
ENSP00000452208.1:n.548G>A
|
|
ENST00000557316.5:c.488G>A
|
ENSP00000452314.1:p.Trp163Ter
|
|
ENST00000622264.4:c.478G>A
|
|
|
NM_000153.3:c.488G>A
|
NP_000144.2:p.Trp163Ter
|
|
NM_001201401.1:c.419G>A
|
NP_001188330.1:p.Trp140Ter
|
|
NM_001201402.1:c.410G>A
|
NP_001188331.1:p.Trp137Ter
|
|
XM_011536618.1:c.320G>A
|
XP_011534920.1:p.Trp107Ter
|
|
XM_011536618.2:c.320G>A
|
XP_011534920.1:p.Trp107Ter
|
|
NM_000153.4:c.488G>A
MANE Select
|
NP_000144.2:p.Trp163Ter
|
|
NM_001201401.2:c.419G>A
|
NP_001188330.1:p.Trp140Ter
|
|
NM_001201402.2:c.410G>A
|
NP_001188331.1:p.Trp137Ter
|
|