|
ENST00000646891.2:c.1766C>G
MANE Select
|
ENSP00000493543.1:p.Thr589Arg
|
|
|
ENST00000288602.11:c.1886C>G
|
ENSP00000288602.7:p.Thr629Arg
|
|
|
ENST00000479537.6:c.436C>G
|
|
|
|
ENST00000496384.7:c.1766C>G
|
ENSP00000419060.2:p.Thr589Arg
|
|
|
ENST00000497784.2:c.*1216C>G
|
ENSP00000420119.2:n.*1216C>G
|
|
|
ENST00000642228.1:c.*844C>G
|
ENSP00000493678.1:n.*844C>G
|
|
|
ENST00000642875.1:n.1259-3951C>G
|
|
|
|
ENST00000644120.1:n.2156C>G
|
|
|
|
ENST00000644650.1:c.862C>G
|
|
|
|
ENST00000644905.1:n.2648C>G
|
|
|
|
ENST00000644969.2:c.1886C>G
MANE Plus Clinical
|
ENSP00000496776.1:p.Thr629Arg
|
|
|
ENST00000646730.1:c.*342C>G
|
ENSP00000494784.1:n.*342C>G
|
|
|
ENST00000646891.1:c.1766C>G
|
ENSP00000493543.1:p.Thr589Arg
|
|
|
ENST00000647434.1:c.738-3951C>G
|
ENSP00000495132.1:n.738-3951C>G
|
|
|
ENST00000288602.10:c.1766C>G
|
ENSP00000288602.6:p.Thr589Arg
|
|
|
ENST00000479537.5:c.50C>G
|
ENSP00000418033.1:p.Thr17Arg
|
|
|
ENST00000496384.6:c.589C>G
|
|
|
|
ENST00000497784.1:c.1801C>G
|
ENSP00000420119.1:n.1801C>G
|
|
|
NM_004333.4:c.1766C>G , LRG_299t1:c.1766C>G
|
NP_004324.2:p.Thr589Arg
|
|
|
XM_005250045.1:c.1766C>G
|
XP_005250102.1:p.Thr589Arg
|
|
|
XM_005250046.1:c.1766C>G
|
XP_005250103.1:p.Thr589Arg
|
|
|
XM_011516529.1:c.1766C>G
|
XP_011514831.1:p.Thr589Arg
|
|
|
XM_011516530.1:c.1695-3951C>G
|
XP_011514832.1:n.1695-3951C>G
|
|
|
XR_242190.1:n.1774C>G
|
|
|
|
XR_927520.1:n.1774C>G
|
|
|
|
XR_927521.1:n.1774C>G
|
|
|
|
XR_927522.1:n.1703-3951C>G
|
|
|
|
XR_927523.1:n.1703-3951C>G
|
|
|
|
NM_001354609.1:c.1766C>G
|
NP_001341538.1:p.Thr589Arg
|
|
|
NM_004333.5:c.1766C>G
|
NP_004324.2:p.Thr589Arg
|
|
|
NR_148928.1:n.2864C>G
|
|
|
|
XM_017012558.1:c.1886C>G
|
XP_016868047.1:p.Thr629Arg
|
|
|
XM_017012559.1:c.1886C>G
|
XP_016868048.1:p.Thr629Arg
|
|
|
XR_001744857.1:n.1894C>G
|
|
|
|
XR_001744858.1:n.1823-3951C>G
|
|
|
|
NM_001354609.2:c.1766C>G
|
NP_001341538.1:p.Thr589Arg
|
|
|
NM_001374244.1:c.1886C>G
|
NP_001361173.1:p.Thr629Arg
|
|
|
NM_001374258.1:c.1886C>G
MANE Plus Clinical
|
NP_001361187.1:p.Thr629Arg
|
|
|
NM_004333.6:c.1766C>G
MANE Select
|
NP_004324.2:p.Thr589Arg
|
|
|
NM_001378467.1:c.1775C>G
|
NP_001365396.1:p.Thr592Arg
|
|
|
NM_001378468.1:c.1766C>G
|
NP_001365397.1:p.Thr589Arg
|
|
|
NM_001378469.1:c.1700C>G
|
NP_001365398.1:p.Thr567Arg
|
|
|
NM_001378470.1:c.1664C>G
|
NP_001365399.1:p.Thr555Arg
|
|
|
NM_001378471.1:c.1655C>G
|
NP_001365400.1:p.Thr552Arg
|
|
|
NM_001378472.1:c.1610C>G
|
NP_001365401.1:p.Thr537Arg
|
|
|
NM_001378473.1:c.1610C>G
|
NP_001365402.1:p.Thr537Arg
|
|
|
NM_001378474.1:c.1766C>G
|
NP_001365403.1:p.Thr589Arg
|
|
|
NM_001378475.1:c.1502C>G
|
NP_001365404.1:p.Thr501Arg
|
|
