|
ENST00000360822.8:c.2952G=
|
ENSP00000354065.4:p.Gln984=
|
|
|
ENST00000416449.6:c.3546G=
|
ENSP00000400395.2:p.Gln1182=
|
|
|
ENST00000479584.2:n.1889G=
|
|
|
|
ENST00000684780.1:n.3932G=
|
|
|
|
ENST00000685866.1:c.*1469G=
|
ENSP00000509484.1:n.*1469G=
|
|
|
ENST00000686376.1:c.3722G=
|
ENSP00000510021.1:n.3722G=
|
|
|
ENST00000686842.1:n.7196G=
|
|
|
|
ENST00000687279.1:c.3639G=
|
ENSP00000508692.1:p.Gln1213=
|
|
|
ENST00000687311.1:n.3605G=
|
|
|
|
ENST00000687633.1:c.3543G=
|
ENSP00000510289.1:p.Gln1181=
|
|
|
ENST00000688923.1:n.3014G=
|
|
|
|
ENST00000689688.1:c.3642G=
|
ENSP00000510155.1:p.Gln1214=
|
|
|
ENST00000690646.1:c.3546G=
|
ENSP00000510383.1:p.Gln1182=
|
|
|
ENST00000690814.1:c.*818G=
|
ENSP00000508792.1:n.*818G=
|
|
|
ENST00000691504.1:n.3536G=
|
|
|
|
ENST00000692155.1:c.3722G=
|
ENSP00000510290.1:n.3722G=
|
|
|
ENST00000692746.1:n.3549G=
|
|
|
|
ENST00000693386.1:c.3546G=
|
ENSP00000510003.1:p.Gln1182=
|
|
|
ENST00000693433.1:n.3536G=
|
|
|
|
ENST00000693714.1:n.3589G=
|
|
|
|
ENST00000693728.1:c.3546G=
|
ENSP00000510580.1:p.Gln1182=
|
|
|
ENST00000349780.9:c.3642G=
MANE Select
|
ENSP00000343818.4:p.Gln1214=
|
|
|
ENST00000349780.8:c.3642G=
|
ENSP00000343818.4:p.Gln1214=
|
|
|
ENST00000360190.8:c.3642G=
|
ENSP00000353317.4:p.Gln1214=
|
|
|
ENST00000360822.7:c.2952G=
|
ENSP00000354065.4:p.Gln984=
|
|
|
ENST00000416449.5:c.1824G=
|
ENSP00000400395.1:p.Gln608=
|
|
|
ENST00000425647.1:c.672G=
|
ENSP00000409941.1:p.Gln224=
|
|
|
ENST00000473282.6:c.*2466G=
|
ENSP00000419265.1:n.*2466G=
|
|
|
ENST00000480112.5:c.*1469G=
|
ENSP00000418418.1:n.*1469G=
|
|
|
ENST00000483412.5:n.2950G=
|
|
|
|
NM_001011649.2:c.3642G=
|
NP_001011649.1:p.Gln1214=
|
|
|
NM_001272039.1:c.2952G=
|
NP_001258968.1:p.Gln984=
|
|
|
NM_018249.5:c.3642G=
|
NP_060719.4:p.Gln1214=
|
|
|
NR_073554.1:n.3911G=
|
|
|
|
NR_073555.1:n.3834G=
|
|
|
|
NR_073556.1:n.4041G=
|
|
|
|
NR_073557.1:n.3914G=
|
|
|
|
NR_073558.1:n.3911G=
|
|
|
|
XM_006717182.1:c.3546G=
|
XP_006717245.1:p.Gln1182=
|
|
|
XM_006717185.1:c.2955G=
|
XP_006717248.1:p.Gln985=
|
|
|
XM_011518860.1:c.3639G=
|
XP_011517162.1:p.Gln1213=
|
|
|
XM_011518861.1:c.3639G=
|
XP_011517163.1:p.Gln1213=
|
|
|
XM_017014921.1:c.3543G=
|
XP_016870410.1:p.Gln1181=
|
|
|
XM_017014922.1:c.2808G=
|
XP_016870411.1:p.Gln936=
|
|
|
XM_017014923.1:c.2955G=
|
XP_016870412.1:p.Gln985=
|
|
|
XM_017014924.1:c.1437G=
|
XP_016870413.1:p.Gln479=
|
|
|
NM_018249.6:c.3642G=
MANE Select
|
NP_060719.4:p.Gln1214=
|
|
|
NM_001011649.3:c.3642G=
|
NP_001011649.1:p.Gln1214=
|
|
|
NR_073554.2:n.3908G=
|
|
|
|
NR_073555.2:n.3831G=
|
|
|
|
NR_073556.2:n.4038G=
|
|
|
|
NR_073557.2:n.3911G=
|
|
|
|
NR_073558.2:n.3908G=
|
|
|
|
NM_001272039.2:c.2952G=
|
NP_001258968.1:p.Gln984=
|
|
