|
ENST00000360822.8:c.2976A=
|
ENSP00000354065.4:p.Gln992=
|
|
|
ENST00000416449.6:c.3570A=
|
ENSP00000400395.2:p.Gln1190=
|
|
|
ENST00000479584.2:n.1913A=
|
|
|
|
ENST00000684780.1:n.3956A=
|
|
|
|
ENST00000685866.1:c.*1493A=
|
ENSP00000509484.1:n.*1493A=
|
|
|
ENST00000686376.1:c.3746A=
|
ENSP00000510021.1:n.3746A=
|
|
|
ENST00000686842.1:n.7220A=
|
|
|
|
ENST00000687279.1:c.3663A=
|
ENSP00000508692.1:p.Gln1221=
|
|
|
ENST00000687311.1:n.3629A=
|
|
|
|
ENST00000687633.1:c.3567A=
|
ENSP00000510289.1:p.Gln1189=
|
|
|
ENST00000688923.1:n.3038A=
|
|
|
|
ENST00000689688.1:c.3666A=
|
ENSP00000510155.1:p.Gln1222=
|
|
|
ENST00000690646.1:c.3570A=
|
ENSP00000510383.1:p.Gln1190=
|
|
|
ENST00000690814.1:c.*842A=
|
ENSP00000508792.1:n.*842A=
|
|
|
ENST00000691504.1:n.3560A=
|
|
|
|
ENST00000692155.1:c.3746A=
|
ENSP00000510290.1:n.3746A=
|
|
|
ENST00000692746.1:n.3573A=
|
|
|
|
ENST00000693386.1:c.3570A=
|
ENSP00000510003.1:p.Gln1190=
|
|
|
ENST00000693433.1:n.3560A=
|
|
|
|
ENST00000693714.1:n.3613A=
|
|
|
|
ENST00000693728.1:c.3570A=
|
ENSP00000510580.1:p.Gln1190=
|
|
|
ENST00000349780.9:c.3666A=
MANE Select
|
ENSP00000343818.4:p.Gln1222=
|
|
|
ENST00000349780.8:c.3666A=
|
ENSP00000343818.4:p.Gln1222=
|
|
|
ENST00000360190.8:c.3666A=
|
ENSP00000353317.4:p.Gln1222=
|
|
|
ENST00000360822.7:c.2976A=
|
ENSP00000354065.4:p.Gln992=
|
|
|
ENST00000416449.5:c.1848A=
|
ENSP00000400395.1:p.Gln616=
|
|
|
ENST00000425647.1:c.696A=
|
ENSP00000409941.1:p.Gln232=
|
|
|
ENST00000473282.6:c.*2490A=
|
ENSP00000419265.1:n.*2490A=
|
|
|
ENST00000480112.5:c.*1493A=
|
ENSP00000418418.1:n.*1493A=
|
|
|
ENST00000483412.5:n.2974A=
|
|
|
|
NM_001011649.2:c.3666A=
|
NP_001011649.1:p.Gln1222=
|
|
|
NM_001272039.1:c.2976A=
|
NP_001258968.1:p.Gln992=
|
|
|
NM_018249.5:c.3666A=
|
NP_060719.4:p.Gln1222=
|
|
|
NR_073554.1:n.3935A=
|
|
|
|
NR_073555.1:n.3858A=
|
|
|
|
NR_073556.1:n.4065A=
|
|
|
|
NR_073557.1:n.3938A=
|
|
|
|
NR_073558.1:n.3935A=
|
|
|
|
XM_006717182.1:c.3570A=
|
XP_006717245.1:p.Gln1190=
|
|
|
XM_006717185.1:c.2979A=
|
XP_006717248.1:p.Gln993=
|
|
|
XM_011518860.1:c.3663A=
|
XP_011517162.1:p.Gln1221=
|
|
|
XM_011518861.1:c.3663A=
|
XP_011517163.1:p.Gln1221=
|
|
|
XM_017014921.1:c.3567A=
|
XP_016870410.1:p.Gln1189=
|
|
|
XM_017014922.1:c.2832A=
|
XP_016870411.1:p.Gln944=
|
|
|
XM_017014923.1:c.2979A=
|
XP_016870412.1:p.Gln993=
|
|
|
XM_017014924.1:c.1461A=
|
XP_016870413.1:p.Gln487=
|
|
|
NM_018249.6:c.3666A=
MANE Select
|
NP_060719.4:p.Gln1222=
|
|
|
NM_001011649.3:c.3666A=
|
NP_001011649.1:p.Gln1222=
|
|
|
NR_073554.2:n.3932A=
|
|
|
|
NR_073555.2:n.3855A=
|
|
|
|
NR_073556.2:n.4062A=
|
|
|
|
NR_073557.2:n.3935A=
|
|
|
|
NR_073558.2:n.3932A=
|
|
|
|
NM_001272039.2:c.2976A=
|
NP_001258968.1:p.Gln992=
|
|
