|
ENST00000413740.2:c.1250C>G
|
ENSP00000416476.2:p.Thr417Arg
|
|
|
ENST00000429117.6:c.956C>G
|
ENSP00000407019.2:p.Thr319Arg
|
|
|
ENST00000450420.6:c.1250C>G
|
ENSP00000393006.2:p.Thr417Arg
|
|
|
ENST00000456676.7:c.1250C>G
|
ENSP00000416687.3:p.Thr417Arg
|
|
|
ENST00000458009.6:c.*151C>G
|
ENSP00000411066.2:n.*151C>G
|
|
|
ENST00000492474.6:c.527C>G
|
ENSP00000518393.1:p.Thr176Arg
|
|
|
ENST00000616768.6:c.1250C>G
|
ENSP00000480669.3:p.Thr417Arg
|
|
|
ENST00000673673.2:c.1250C>G
|
ENSP00000500979.2:p.Thr417Arg
|
|
|
ENST00000231790.8:c.1250C>G
MANE Select
|
ENSP00000231790.3:p.Thr417Arg
|
|
|
ENST00000413212.2:c.*168C>G
|
ENSP00000400844.2:n.*168C>G
|
|
|
ENST00000432299.6:c.*1082C>G
|
ENSP00000416783.1:n.*1082C>G
|
|
|
ENST00000441265.6:c.527C>G
|
ENSP00000398392.2:p.Thr176Arg
|
|
|
ENST00000442249.6:n.1058C>G
|
|
|
|
ENST00000447829.6:c.*361C>G
|
ENSP00000399329.2:n.*361C>G
|
|
|
ENST00000539477.6:c.527C>G
|
ENSP00000443665.1:p.Thr176Arg
|
|
|
ENST00000616768.5:c.287C>G
|
ENSP00000480669.2:p.Thr96Arg
|
|
|
ENST00000673673.1:c.1203C>G
|
|
|
|
ENST00000673713.1:n.1374C>G
|
|
|
|
ENST00000673715.1:c.1250C>G
|
ENSP00000501301.1:p.Thr417Arg
|
|
|
ENST00000673889.1:n.632C>G
|
|
|
|
ENST00000673897.1:c.*1042C>G
|
ENSP00000501109.1:n.*1042C>G
|
|
|
ENST00000673899.1:c.678-2936C>G
|
ENSP00000501030.1:n.678-2936C>G
|
|
|
ENST00000673947.1:c.*1390C>G
|
ENSP00000501304.1:n.*1390C>G
|
|
|
ENST00000673972.1:c.*1128C>G
|
ENSP00000501281.1:n.*1128C>G
|
|
|
ENST00000673990.1:n.1141C>G
|
|
|
|
ENST00000674019.1:c.527C>G
|
ENSP00000501081.1:p.Thr176Arg
|
|
|
ENST00000674107.1:n.1098C>G
|
|
|
|
ENST00000674111.1:c.1250C>G
|
ENSP00000501162.1:p.Thr417Arg
|
|
|
ENST00000231790.6:c.1250C>G
|
ENSP00000231790.2:p.Thr417Arg
|
|
|
ENST00000413212.1:c.325C>G
|
|
|
|
ENST00000435176.5:c.956C>G
|
ENSP00000402564.1:p.Thr319Arg
|
|
|
ENST00000447829.5:c.537C>G
|
|
|
|
ENST00000455445.6:c.527C>G
|
ENSP00000398272.2:p.Thr176Arg
|
|
|
ENST00000456676.6:c.1225C>G
|
|
|
|
ENST00000458009.5:c.437C>G
|
|
|
|
ENST00000458205.6:c.527C>G
|
ENSP00000402667.2:p.Thr176Arg
|
|
|
ENST00000536378.5:c.527C>G
|
ENSP00000444286.2:p.Thr176Arg
|
|
|
ENST00000539477.5:c.527C>G
|
ENSP00000443665.1:p.Thr176Arg
|
|
|
ENST00000616768.4:c.18C>G
|
|
|
|
NM_000249.3:c.1250C>G , LRG_216t1:c.1250C>G
|
NP_000240.1:p.Thr417Arg
|
|
|
NM_001167617.1:c.956C>G
|
NP_001161089.1:p.Thr319Arg
|
|
|
NM_001167618.1:c.527C>G
|
NP_001161090.1:p.Thr176Arg
|
|
|
NM_001167619.1:c.527C>G
|
NP_001161091.1:p.Thr176Arg
|
|
|
NM_001258271.1:c.1250C>G
|
NP_001245200.1:p.Thr417Arg
|
|
|
NM_001258273.1:c.527C>G
|
NP_001245202.1:p.Thr176Arg
|
|
|
NM_001258274.1:c.527C>G
|
NP_001245203.1:p.Thr176Arg
|
|
|
XM_005265161.1:c.1043C>G
|
XP_005265218.1:p.Thr348Arg
|
|
|
XM_005265163.1:c.527C>G
|
XP_005265220.1:p.Thr176Arg
|
|
|
XM_005265164.1:c.527C>G
|
XP_005265221.1:p.Thr176Arg
|
|
|
XM_005265166.1:c.227C>G
|
XP_005265223.1:p.Thr76Arg
|
|
|
XM_011533727.1:c.176C>G
|
XP_011532029.1:p.Thr59Arg
|
|
|
NM_001167617.2:c.956C>G
|
NP_001161089.1:p.Thr319Arg
|
|
|
NM_001167618.2:c.527C>G
|
NP_001161090.1:p.Thr176Arg
|
|
|
NM_001167619.2:c.527C>G
|
NP_001161091.1:p.Thr176Arg
|
|
|
NM_001258274.2:c.527C>G
|
NP_001245203.1:p.Thr176Arg
|
|
|
NM_001354615.1:c.527C>G
|
NP_001341544.1:p.Thr176Arg
|
|
|
NM_001354616.1:c.527C>G
|
NP_001341545.1:p.Thr176Arg
|
|
|
NM_001354617.1:c.527C>G
|
NP_001341546.1:p.Thr176Arg
|
|
|
NM_001354618.1:c.527C>G
|
NP_001341547.1:p.Thr176Arg
|
|
|
NM_001354619.1:c.527C>G
|
NP_001341548.1:p.Thr176Arg
|
|
|
NM_001354620.1:c.956C>G
|
NP_001341549.1:p.Thr319Arg
|
|
|
NM_001354621.1:c.227C>G
|
NP_001341550.1:p.Thr76Arg
|
|
|
NM_001354622.1:c.227C>G
|
NP_001341551.1:p.Thr76Arg
|
|
|
NM_001354623.1:c.227C>G
|
NP_001341552.1:p.Thr76Arg
|
|
|
NM_001354624.1:c.176C>G
|
NP_001341553.1:p.Thr59Arg
|
|
|
NM_001354625.1:c.176C>G
|
NP_001341554.1:p.Thr59Arg
|
|
|
NM_001354626.1:c.176C>G
|
NP_001341555.1:p.Thr59Arg
|
|
|
NM_001354627.1:c.176C>G
|
NP_001341556.1:p.Thr59Arg
|
|
|
NM_001354628.1:c.1250C>G
|
NP_001341557.1:p.Thr417Arg
|
|
|
NM_001354629.1:c.1151C>G
|
NP_001341558.1:p.Thr384Arg
|
|
|
NM_001354630.1:c.1250C>G
|
NP_001341559.1:p.Thr417Arg
|
|
|
XM_005265161.2:c.1043C>G
|
XP_005265218.1:p.Thr348Arg
|
|
|
XM_017006450.2:c.227C>G
|
XP_016861939.1:p.Thr76Arg
|
|
|
NM_000249.4:c.1250C>G
MANE Select
|
NP_000240.1:p.Thr417Arg
|
|
|
NM_001167617.3:c.956C>G
|
NP_001161089.1:p.Thr319Arg
|
|
|
NM_001167618.3:c.527C>G
|
NP_001161090.1:p.Thr176Arg
|
|
|
NM_001167619.3:c.527C>G
|
NP_001161091.1:p.Thr176Arg
|
|
|
NM_001258271.2:c.1250C>G
|
NP_001245200.1:p.Thr417Arg
|
|
|
NM_001258273.2:c.527C>G
|
NP_001245202.1:p.Thr176Arg
|
|
|
NM_001258274.3:c.527C>G
|
NP_001245203.1:p.Thr176Arg
|
|
|
NM_001354615.2:c.527C>G
|
NP_001341544.1:p.Thr176Arg
|
|
|
NM_001354616.2:c.527C>G
|
NP_001341545.1:p.Thr176Arg
|
|
|
NM_001354617.2:c.527C>G
|
NP_001341546.1:p.Thr176Arg
|
|
|
NM_001354618.2:c.527C>G
|
NP_001341547.1:p.Thr176Arg
|
|
|
NM_001354619.2:c.527C>G
|
NP_001341548.1:p.Thr176Arg
|
|
|
NM_001354620.2:c.956C>G
|
NP_001341549.1:p.Thr319Arg
|
|
|
NM_001354621.2:c.227C>G
|
NP_001341550.1:p.Thr76Arg
|
|
|
NM_001354622.2:c.227C>G
|
NP_001341551.1:p.Thr76Arg
|
|
|
NM_001354623.2:c.227C>G
|
NP_001341552.1:p.Thr76Arg
|
|
|
NM_001354624.2:c.176C>G
|
NP_001341553.1:p.Thr59Arg
|
|
|
NM_001354625.2:c.176C>G
|
NP_001341554.1:p.Thr59Arg
|
|
|
NM_001354626.2:c.176C>G
|
NP_001341555.1:p.Thr59Arg
|
|
|
NM_001354627.2:c.176C>G
|
NP_001341556.1:p.Thr59Arg
|
|
|
NM_001354628.2:c.1250C>G
|
NP_001341557.1:p.Thr417Arg
|
|
|
NM_001354629.2:c.1151C>G
|
NP_001341558.1:p.Thr384Arg
|
|
|
NM_001354630.2:c.1250C>G
|
NP_001341559.1:p.Thr417Arg
|
|
