|
ENST00000646891.2:c.1726G>T
MANE Select
|
ENSP00000493543.1:p.Asp576Tyr
|
|
|
ENST00000288602.11:c.1846G>T
|
ENSP00000288602.7:p.Asp616Tyr
|
|
|
ENST00000479537.6:c.396G>T
|
|
|
|
ENST00000496384.7:c.1726G>T
|
ENSP00000419060.2:p.Asp576Tyr
|
|
|
ENST00000497784.2:c.*1176G>T
|
ENSP00000420119.2:n.*1176G>T
|
|
|
ENST00000642228.1:c.*804G>T
|
ENSP00000493678.1:n.*804G>T
|
|
|
ENST00000642875.1:n.1259-4784G>T
|
|
|
|
ENST00000644120.1:n.2116G>T
|
|
|
|
ENST00000644650.1:c.822G>T
|
|
|
|
ENST00000644905.1:n.1815G>T
|
|
|
|
ENST00000644969.2:c.1846G>T
MANE Plus Clinical
|
ENSP00000496776.1:p.Asp616Tyr
|
|
|
ENST00000646730.1:c.*302G>T
|
ENSP00000494784.1:n.*302G>T
|
|
|
ENST00000646891.1:c.1726G>T
|
ENSP00000493543.1:p.Asp576Tyr
|
|
|
ENST00000647434.1:c.738-4784G>T
|
ENSP00000495132.1:n.738-4784G>T
|
|
|
ENST00000288602.10:c.1726G>T
|
ENSP00000288602.6:p.Asp576Tyr
|
|
|
ENST00000479537.5:c.10G>T
|
ENSP00000418033.1:p.Asp4Tyr
|
|
|
ENST00000496384.6:c.549G>T
|
|
|
|
ENST00000497784.1:c.1761G>T
|
ENSP00000420119.1:n.1761G>T
|
|
|
NM_004333.4:c.1726G>T , LRG_299t1:c.1726G>T
|
NP_004324.2:p.Asp576Tyr
|
|
|
XM_005250045.1:c.1726G>T
|
XP_005250102.1:p.Asp576Tyr
|
|
|
XM_005250046.1:c.1726G>T
|
XP_005250103.1:p.Asp576Tyr
|
|
|
XM_011516529.1:c.1726G>T
|
XP_011514831.1:p.Asp576Tyr
|
|
|
XM_011516530.1:c.1695-4784G>T
|
XP_011514832.1:n.1695-4784G>T
|
|
|
XR_242190.1:n.1734G>T
|
|
|
|
XR_927520.1:n.1734G>T
|
|
|
|
XR_927521.1:n.1734G>T
|
|
|
|
XR_927522.1:n.1703-4784G>T
|
|
|
|
XR_927523.1:n.1703-4784G>T
|
|
|
|
NM_001354609.1:c.1726G>T
|
NP_001341538.1:p.Asp576Tyr
|
|
|
NM_004333.5:c.1726G>T
|
NP_004324.2:p.Asp576Tyr
|
|
|
NR_148928.1:n.2031G>T
|
|
|
|
XM_017012558.1:c.1846G>T
|
XP_016868047.1:p.Asp616Tyr
|
|
|
XM_017012559.1:c.1846G>T
|
XP_016868048.1:p.Asp616Tyr
|
|
|
XR_001744857.1:n.1854G>T
|
|
|
|
XR_001744858.1:n.1823-4784G>T
|
|
|
|
NM_001354609.2:c.1726G>T
|
NP_001341538.1:p.Asp576Tyr
|
|
|
NM_001374244.1:c.1846G>T
|
NP_001361173.1:p.Asp616Tyr
|
|
|
NM_001374258.1:c.1846G>T
MANE Plus Clinical
|
NP_001361187.1:p.Asp616Tyr
|
|
|
NM_004333.6:c.1726G>T
MANE Select
|
NP_004324.2:p.Asp576Tyr
|
|
|
NM_001378467.1:c.1735G>T
|
NP_001365396.1:p.Asp579Tyr
|
|
|
NM_001378468.1:c.1726G>T
|
NP_001365397.1:p.Asp576Tyr
|
|
|
NM_001378469.1:c.1660G>T
|
NP_001365398.1:p.Asp554Tyr
|
|
|
NM_001378470.1:c.1624G>T
|
NP_001365399.1:p.Asp542Tyr
|
|
|
NM_001378471.1:c.1615G>T
|
NP_001365400.1:p.Asp539Tyr
|
|
|
NM_001378472.1:c.1570G>T
|
NP_001365401.1:p.Asp524Tyr
|
|
|
NM_001378473.1:c.1570G>T
|
NP_001365402.1:p.Asp524Tyr
|
|
|
NM_001378474.1:c.1726G>T
|
NP_001365403.1:p.Asp576Tyr
|
|
|
NM_001378475.1:c.1462G>T
|
NP_001365404.1:p.Asp488Tyr
|
|
