|
ENST00000260570.8:c.905G>T
MANE Select
|
ENSP00000260570.3:p.Cys302Phe
|
|
|
ENST00000476264.7:n.1194G>T
|
|
|
|
ENST00000674701.1:c.905G>T
|
ENSP00000502275.1:p.Cys302Phe
|
|
|
ENST00000674824.1:c.842G>T
|
ENSP00000501824.1:p.Cys281Phe
|
|
|
ENST00000674932.1:c.*568G>T
|
ENSP00000501967.1:n.*568G>T
|
|
|
ENST00000675410.1:c.224G>T
|
ENSP00000502030.1:p.Cys75Phe
|
|
|
ENST00000675618.1:n.985G>T
|
|
|
|
ENST00000675690.1:c.905G>T
|
ENSP00000502283.1:p.Cys302Phe
|
|
|
ENST00000675728.1:c.842G>T
|
ENSP00000501700.1:p.Cys281Phe
|
|
|
ENST00000675729.1:c.905G>T
|
ENSP00000502319.1:p.Cys302Phe
|
|
|
ENST00000675963.1:c.*603G>T
|
ENSP00000502708.1:n.*603G>T
|
|
|
ENST00000676119.1:c.*195G>T
|
ENSP00000501701.1:n.*195G>T
|
|
|
ENST00000676300.1:n.991G>T
|
|
|
|
ENST00000260570.7:c.905G>T
|
ENSP00000260570.3:p.Cys302Phe
|
|
|
ENST00000359466.10:c.905G>T
|
ENSP00000352443.6:p.Cys302Phe
|
|
|
ENST00000416524.2:c.842G>T
|
ENSP00000407408.2:p.Cys281Phe
|
|
|
ENST00000476264.6:n.851G>T
|
|
|
|
ENST00000507184.5:n.1037G>T
|
|
|
|
ENST00000511842.5:n.930G>T
|
|
|
|
NM_015662.2:c.905G>T
|
NP_056477.1:p.Cys302Phe
|
|
|
XM_005264254.1:c.905G>T
|
XP_005264311.1:p.Cys302Phe
|
|
|
XM_006711986.2:c.842G>T
|
XP_006712049.1:p.Cys281Phe
|
|
|
XM_006711987.1:c.905G>T
|
XP_006712050.1:p.Cys302Phe
|
|
|
XM_011532757.1:c.224G>T
|
XP_011531059.1:p.Cys75Phe
|
|
|
XM_011532758.1:c.905G>T
|
XP_011531060.1:p.Cys302Phe
|
|
|
XM_006711986.3:c.842G>T
|
XP_006712049.1:p.Cys281Phe
|
|
|
XM_011532757.2:c.224G>T
|
XP_011531059.1:p.Cys75Phe
|
|
|
XM_017003790.1:c.842G>T
|
XP_016859279.1:p.Cys281Phe
|
|
|
XM_017003791.1:c.224G>T
|
XP_016859280.1:p.Cys75Phe
|
|
|
XM_017003792.1:c.905G>T
|
XP_016859281.1:p.Cys302Phe
|
|
|
XM_017003793.1:c.-546G>T
|
XP_016859282.1:n.-546G>T
|
|
|
XM_017003794.1:c.-546G>T
|
XP_016859283.1:n.-546G>T
|
|
|
XM_017003795.1:c.-918G>T
|
XP_016859284.1:n.-918G>T
|
|
|
XR_001738698.1:n.960G>T
|
|
|
|
NM_015662.3:c.905G>T
MANE Select
|
NP_056477.1:p.Cys302Phe
|
|
