|
ENST00000460843.6:c.1922C>G
MANE Select
|
ENSP00000417980.1:p.Thr641Arg
|
|
|
ENST00000636027.1:c.1808C>G
|
ENSP00000489961.1:p.Thr603Arg
|
|
|
ENST00000637161.1:c.1829C>G
|
ENSP00000490328.1:p.Thr610Arg
|
|
|
ENST00000637261.1:c.1962C>G
|
ENSP00000490815.1:n.1962C>G
|
|
|
ENST00000638071.1:c.1549C>G
|
|
|
|
ENST00000640639.1:c.1091C>G
|
ENSP00000491823.1:p.Thr364Arg
|
|
|
ENST00000371394.6:c.*1657C>G
|
ENSP00000485945.1:n.*1657C>G
|
|
|
ENST00000460843.5:c.1922C>G
|
ENSP00000417980.1:p.Thr641Arg
|
|
|
ENST00000462484.5:c.1922C>G
|
ENSP00000417328.1:p.Thr641Arg
|
|
|
ENST00000462942.3:c.779C>G
|
ENSP00000436107.1:p.Thr260Arg
|
|
|
ENST00000465566.2:c.470C>G
|
ENSP00000486261.1:p.Thr157Arg
|
|
|
ENST00000626603.1:n.1701G>C
|
|
|
|
NM_001145527.1:c.1922C>G
|
NP_001138999.1:p.Thr641Arg
|
|
|
NM_024757.4:c.1922C>G
|
NP_079033.4:p.Thr641Arg
|
|
|
XM_005266105.3:c.1913C>G
|
XP_005266162.1:p.Thr638Arg
|
|
|
XM_005266110.1:c.1829C>G
|
XP_005266167.1:p.Thr610Arg
|
|
|
XM_006717288.2:c.1904C>G
|
XP_006717351.1:p.Thr635Arg
|
|
|
XM_011519021.1:c.1931C>G
|
XP_011517323.1:p.Thr644Arg
|
|
|
XM_011519022.1:c.1928C>G
|
XP_011517324.1:p.Thr643Arg
|
|
|
XM_011519023.1:c.1910C>G
|
XP_011517325.1:p.Thr637Arg
|
|
|
XM_011519024.1:c.1853C>G
|
XP_011517326.1:p.Thr618Arg
|
|
|
XM_011519025.1:c.1829C>G
|
XP_011517327.1:p.Thr610Arg
|
|
|
XM_011519026.1:c.1787C>G
|
XP_011517328.1:p.Thr596Arg
|
|
|
XM_011519027.1:c.1931C>G
|
XP_011517329.1:p.Thr644Arg
|
|
|
XM_011519028.1:c.1931C>G
|
XP_011517330.1:p.Thr644Arg
|
|
|
XM_011519029.1:c.353C>G
|
XP_011517331.1:p.Thr118Arg
|
|
|
XM_011519033.1:c.1766C>G
|
XP_011517335.1:p.Thr589Arg
|
|
|
NM_001354259.1:c.1829C>G
|
NP_001341188.1:p.Thr610Arg
|
|
|
NM_001354263.1:c.1901C>G
|
NP_001341192.1:p.Thr634Arg
|
|
|
XM_005266105.5:c.1913C>G
|
XP_005266162.1:p.Thr638Arg
|
|
|
XM_011519021.3:c.1931C>G
|
XP_011517323.1:p.Thr644Arg
|
|
|
XM_011519022.3:c.1928C>G
|
XP_011517324.1:p.Thr643Arg
|
|
|
XM_011519023.3:c.1910C>G
|
XP_011517325.1:p.Thr637Arg
|
|
|
XM_011519029.3:c.353C>G
|
XP_011517331.1:p.Thr118Arg
|
|
|
XM_017015134.1:c.1907C>G
|
XP_016870623.1:p.Thr636Arg
|
|
|
XM_017015136.2:c.1823C>G
|
XP_016870625.1:p.Thr608Arg
|
|
|
XM_017015137.1:c.1808C>G
|
XP_016870626.1:p.Thr603Arg
|
|
|
XM_017015138.1:c.1808C>G
|
XP_016870627.1:p.Thr603Arg
|
|
|
XM_024447674.1:c.1751C>G
|
XP_024303442.1:p.Thr584Arg
|
|
|
XM_024447675.1:c.1685C>G
|
XP_024303443.1:p.Thr562Arg
|
|
|
XM_024447676.1:c.1046C>G
|
XP_024303444.1:p.Thr349Arg
|
|
|
XM_024447677.1:c.1046C>G
|
XP_024303445.1:p.Thr349Arg
|
|
|
XM_024447678.1:c.1829C>G
|
XP_024303446.1:p.Thr610Arg
|
|
|
XM_024447679.1:c.1829C>G
|
XP_024303447.1:p.Thr610Arg
|
|
|
XM_024447680.1:c.1664C>G
|
XP_024303448.1:p.Thr555Arg
|
|
|
NM_024757.5:c.1922C>G
MANE Select
|
NP_079033.4:p.Thr641Arg
|
|
|
NM_001145527.2:c.1922C>G
|
NP_001138999.1:p.Thr641Arg
|
|
|
NM_001354259.2:c.1829C>G
|
NP_001341188.1:p.Thr610Arg
|
|
|
NM_001354263.2:c.1901C>G
|
NP_001341192.1:p.Thr634Arg
|
|
