|
ENST00000646891.2:c.1798_1799insAGACTACAG
MANE Select
|
ENSP00000493543.1:p.Thr599_Val600insGluThrThr
|
|
|
ENST00000288602.11:c.1918_1919insAGACTACAG
|
ENSP00000288602.7:p.Thr639_Val640insGluThrThr
|
|
|
ENST00000479537.6:c.468_469insAGACTACAG
|
|
|
|
ENST00000496384.7:c.1798_1799insAGACTACAG
|
ENSP00000419060.2:p.Thr599_Val600insGluThrThr
|
|
|
ENST00000497784.2:c.*1248_*1249insAGACTACAG
|
ENSP00000420119.2:n.*1248_*1249insAGACTACAG
|
|
|
ENST00000642228.1:c.*876_*877insAGACTACAG
|
ENSP00000493678.1:n.*876_*877insAGACTACAG
|
|
|
ENST00000642875.1:n.1259-3919_1259-3918insAGACTACAG
|
|
|
|
ENST00000644120.1:n.2188_2189insAGACTACAG
|
|
|
|
ENST00000644650.1:c.894_895insAGACTACAG
|
|
|
|
ENST00000644905.1:n.2680_2681insAGACTACAG
|
|
|
|
ENST00000644969.2:c.1918_1919insAGACTACAG
MANE Plus Clinical
|
ENSP00000496776.1:p.Thr639_Val640insGluThrThr
|
|
|
ENST00000646730.1:c.*374_*375insAGACTACAG
|
ENSP00000494784.1:n.*374_*375insAGACTACAG
|
|
|
ENST00000646891.1:c.1798_1799insAGACTACAG
|
ENSP00000493543.1:p.Thr599_Val600insGluThrThr
|
|
|
ENST00000647434.1:c.738-3919_738-3918insAGACTACAG
|
ENSP00000495132.1:n.738-3919_738-3918insAGACTACAG
|
|
|
ENST00000288602.10:c.1798_1799insAGACTACAG
|
ENSP00000288602.6:p.Thr599_Val600insGluThrThr
|
|
|
ENST00000479537.5:c.82_83insAGACTACAG
|
ENSP00000418033.1:p.Thr27_Val28insGluThrThr
|
|
|
ENST00000496384.6:c.621_622insAGACTACAG
|
|
|
|
ENST00000497784.1:c.1833_1834insAGACTACAG
|
ENSP00000420119.1:n.1833_1834insAGACTACAG
|
|
|
NM_004333.4:c.1798_1799insAGACTACAG , LRG_299t1:c.1798_1799insAGACTACAG
|
NP_004324.2:p.Thr599_Val600insGluThrThr
|
|
|
XM_005250045.1:c.1798_1799insAGACTACAG
|
XP_005250102.1:p.Thr599_Val600insGluThrThr
|
|
|
XM_005250046.1:c.1798_1799insAGACTACAG
|
XP_005250103.1:p.Thr599_Val600insGluThrThr
|
|
|
XM_011516529.1:c.1798_1799insAGACTACAG
|
XP_011514831.1:p.Thr599_Val600insGluThrThr
|
|
|
XM_011516530.1:c.1695-3919_1695-3918insAGACTACAG
|
XP_011514832.1:n.1695-3919_1695-3918insAGACTACAG
|
|
|
XR_242190.1:n.1806_1807insAGACTACAG
|
|
|
|
XR_927520.1:n.1806_1807insAGACTACAG
|
|
|
|
XR_927521.1:n.1806_1807insAGACTACAG
|
|
|
|
XR_927522.1:n.1703-3919_1703-3918insAGACTACAG
|
|
|
|
XR_927523.1:n.1703-3919_1703-3918insAGACTACAG
|
|
|
|
NM_001354609.1:c.1798_1799insAGACTACAG
|
NP_001341538.1:p.Thr599_Val600insGluThrThr
|
|
|
NM_004333.5:c.1798_1799insAGACTACAG
|
NP_004324.2:p.Thr599_Val600insGluThrThr
|
|
|
NR_148928.1:n.2896_2897insAGACTACAG
|
|
|
|
XM_017012558.1:c.1918_1919insAGACTACAG
|
XP_016868047.1:p.Thr639_Val640insGluThrThr
|
|
|
XM_017012559.1:c.1918_1919insAGACTACAG
|
XP_016868048.1:p.Thr639_Val640insGluThrThr
|
|
|
XR_001744857.1:n.1926_1927insAGACTACAG
|
|
|
|
XR_001744858.1:n.1823-3919_1823-3918insAGACTACAG
|
|
|
|
NM_001354609.2:c.1798_1799insAGACTACAG
|
NP_001341538.1:p.Thr599_Val600insGluThrThr
|
|
|
NM_001374244.1:c.1918_1919insAGACTACAG
|
NP_001361173.1:p.Thr639_Val640insGluThrThr
|
|
|
NM_001374258.1:c.1918_1919insAGACTACAG
MANE Plus Clinical
|
NP_001361187.1:p.Thr639_Val640insGluThrThr
|
|
|
NM_004333.6:c.1798_1799insAGACTACAG
MANE Select
|
NP_004324.2:p.Thr599_Val600insGluThrThr
|
|
|
NM_001378467.1:c.1807_1808insAGACTACAG
|
NP_001365396.1:p.Thr602_Val603insGluThrThr
|
|
|
NM_001378468.1:c.1798_1799insAGACTACAG
|
NP_001365397.1:p.Thr599_Val600insGluThrThr
|
|
|
NM_001378469.1:c.1732_1733insAGACTACAG
|
NP_001365398.1:p.Thr577_Val578insGluThrThr
|
|
|
NM_001378470.1:c.1696_1697insAGACTACAG
|
NP_001365399.1:p.Thr565_Val566insGluThrThr
|
|
|
NM_001378471.1:c.1687_1688insAGACTACAG
|
NP_001365400.1:p.Thr562_Val563insGluThrThr
|
|
|
NM_001378472.1:c.1642_1643insAGACTACAG
|
NP_001365401.1:p.Thr547_Val548insGluThrThr
|
|
|
NM_001378473.1:c.1642_1643insAGACTACAG
|
NP_001365402.1:p.Thr547_Val548insGluThrThr
|
|
|
NM_001378474.1:c.1798_1799insAGACTACAG
|
NP_001365403.1:p.Thr599_Val600insGluThrThr
|
|
|
NM_001378475.1:c.1534_1535insAGACTACAG
|
NP_001365404.1:p.Thr511_Val512insGluThrThr
|
|
