ENST00000366577.10:c.1700C>G
MANE Select
|
ENSP00000355536.5:p.Thr567Arg
|
|
ENST00000535889.6:c.1700C>G
|
ENSP00000441845.1:p.Thr567Arg
|
|
ENST00000650888.1:c.*742C>G
|
ENSP00000498393.1:n.*742C>G
|
|
ENST00000651455.1:c.*444C>G
|
ENSP00000498963.1:n.*444C>G
|
|
ENST00000674797.2:c.1352C>G
|
ENSP00000502299.2:p.Thr451Arg
|
|
ENST00000679569.1:n.2014C>G
|
|
|
ENST00000679842.1:c.1700C>G
|
ENSP00000506109.1:p.Thr567Arg
|
|
ENST00000680454.1:n.2144C>G
|
|
|
ENST00000681102.1:c.1520C>G
|
ENSP00000505600.1:p.Thr507Arg
|
|
ENST00000681177.1:c.1516-7308C>G
|
ENSP00000506327.1:n.1516-7308C>G
|
|
ENST00000681937.1:n.2148-7308C>G
|
|
|
ENST00000366576.3:c.362C>G
|
ENSP00000355535.3:p.Thr121Arg
|
|
ENST00000366577.9:c.1700C>G
|
ENSP00000355536.5:p.Thr567Arg
|
|
ENST00000463959.1:n.1719C>G
|
|
|
ENST00000535889.5:c.1700C>G
|
ENSP00000441845.1:p.Thr567Arg
|
|
NM_000254.2:c.1700C>G
|
NP_000245.2:p.Thr567Arg
|
|
NM_001291939.1:c.1700C>G
|
NP_001278868.1:p.Thr567Arg
|
|
NM_001291940.1:c.479C>G
|
NP_001278869.1:p.Thr160Arg
|
|
XM_005273141.3:c.1697C>G
|
XP_005273198.1:p.Thr566Arg
|
|
XM_006711769.2:c.1700C>G
|
XP_006711832.1:p.Thr567Arg
|
|
XM_006711770.1:c.764C>G
|
XP_006711833.1:p.Thr255Arg
|
|
XM_011544193.1:c.1700C>G
|
XP_011542495.1:p.Thr567Arg
|
|
XM_011544194.1:c.1868C>G
|
XP_011542496.1:p.Thr623Arg
|
|
XM_005273141.5:c.1697C>G
|
XP_005273198.1:p.Thr566Arg
|
|
XM_006711770.3:c.764C>G
|
XP_006711833.1:p.Thr255Arg
|
|
XM_011544194.3:c.1868C>G
|
XP_011542496.1:p.Thr623Arg
|
|
XM_017001329.2:c.1868C>G
|
XP_016856818.1:p.Thr623Arg
|
|
XM_017001330.2:c.1868C>G
|
XP_016856819.1:p.Thr623Arg
|
|
NM_001291940.2:c.479C>G
|
NP_001278869.1:p.Thr160Arg
|
|
NM_000254.3:c.1700C>G
MANE Select
|
NP_000245.2:p.Thr567Arg
|
|