|
NM_015662.3:c.4642C>T
MANE Select
|
NP_056477.1:p.Gln1548Ter
|
|
ENST00000260570.8:c.4642C>T
MANE Select
|
ENSP00000260570.3:p.Gln1548Ter
|
|
NM_015662.2:c.4642C>T
|
NP_056477.1:p.Gln1548Ter
|
|
ENST00000260570.7:c.4642C>T
|
ENSP00000260570.3:p.Gln1548Ter
|
|
ENST00000420854.1:c.214C>T
|
ENSP00000398633.1:p.Gln72Ter
|
|
ENST00000480892.1:n.45C>T
|
|
|
ENST00000507184.5:n.4923C>T
|
|
|
ENST00000509128.5:c.1060C>T
|
|
|
ENST00000674594.1:n.1254C>T
|
|
|
ENST00000674701.1:c.*4155C>T
|
ENSP00000502275.1:n.*4155C>T
|
|
ENST00000674824.1:c.*3090C>T
|
ENSP00000501824.1:n.*3090C>T
|
|
ENST00000674932.1:c.*5088C>T
|
ENSP00000501967.1:n.*5088C>T
|
|
ENST00000675410.1:c.*2631C>T
|
ENSP00000502030.1:n.*2631C>T
|
|
ENST00000675690.1:c.4576C>T
|
ENSP00000502283.1:p.Gln1526Ter
|
|
ENST00000676119.1:c.*3868C>T
|
ENSP00000501701.1:n.*3868C>T
|
|
XM_005264254.1:c.4576C>T
|
XP_005264311.1:p.Gln1526Ter
|
|
XM_006711986.2:c.4579C>T
|
XP_006712049.1:p.Gln1527Ter
|
|
XM_006711986.3:c.4579C>T
|
XP_006712049.1:p.Gln1527Ter
|
|
XM_006711987.1:c.4642C>T
|
XP_006712050.1:p.Gln1548Ter
|
|
XM_011532757.1:c.3961C>T
|
XP_011531059.1:p.Gln1321Ter
|
|
XM_011532757.2:c.3961C>T
|
XP_011531059.1:p.Gln1321Ter
|
|
XM_011532759.1:c.3082C>T
|
XP_011531061.1:p.Gln1028Ter
|
|
XM_011532759.2:c.3082C>T
|
XP_011531061.1:p.Gln1028Ter
|
|
XM_011532760.1:c.2707C>T
|
XP_011531062.1:p.Gln903Ter
|
|
XM_011532760.2:c.2707C>T
|
XP_011531062.1:p.Gln903Ter
|
|
XM_017003790.1:c.4513C>T
|
XP_016859279.1:p.Gln1505Ter
|
|
XM_017003791.1:c.3961C>T
|
XP_016859280.1:p.Gln1321Ter
|
|
XM_017003793.1:c.2779C>T
|
XP_016859282.1:p.Gln927Ter
|
|
XM_017003794.1:c.2779C>T
|
XP_016859283.1:p.Gln927Ter
|
|
XM_017003795.1:c.2575C>T
|
XP_016859284.1:p.Gln859Ter
|
