|
ENST00000646891.2:c.1837T>G
MANE Select
|
ENSP00000493543.1:p.Leu613Val
|
|
|
ENST00000288602.11:c.1957T>G
|
ENSP00000288602.7:p.Leu653Val
|
|
|
ENST00000479537.6:c.507T>G
|
|
|
|
ENST00000496384.7:c.1837T>G
|
ENSP00000419060.2:p.Leu613Val
|
|
|
ENST00000497784.2:c.*1287T>G
|
ENSP00000420119.2:n.*1287T>G
|
|
|
ENST00000642228.1:c.*915T>G
|
ENSP00000493678.1:n.*915T>G
|
|
|
ENST00000642875.1:n.1259-3880T>G
|
|
|
|
ENST00000644120.1:n.2227T>G
|
|
|
|
ENST00000644650.1:c.933T>G
|
|
|
|
ENST00000644905.1:n.2719T>G
|
|
|
|
ENST00000644969.2:c.1957T>G
MANE Plus Clinical
|
ENSP00000496776.1:p.Leu653Val
|
|
|
ENST00000646730.1:c.*413T>G
|
ENSP00000494784.1:n.*413T>G
|
|
|
ENST00000646891.1:c.1837T>G
|
ENSP00000493543.1:p.Leu613Val
|
|
|
ENST00000647434.1:c.738-3880T>G
|
ENSP00000495132.1:n.738-3880T>G
|
|
|
ENST00000288602.10:c.1837T>G
|
ENSP00000288602.6:p.Leu613Val
|
|
|
ENST00000479537.5:c.121T>G
|
ENSP00000418033.1:p.Leu41Val
|
|
|
ENST00000496384.6:c.660T>G
|
|
|
|
ENST00000497784.1:c.1872T>G
|
ENSP00000420119.1:n.1872T>G
|
|
|
NM_004333.4:c.1837T>G , LRG_299t1:c.1837T>G
|
NP_004324.2:p.Leu613Val
|
|
|
XM_005250045.1:c.1837T>G
|
XP_005250102.1:p.Leu613Val
|
|
|
XM_005250046.1:c.1837T>G
|
XP_005250103.1:p.Leu613Val
|
|
|
XM_011516529.1:c.1837T>G
|
XP_011514831.1:p.Leu613Val
|
|
|
XM_011516530.1:c.1695-3880T>G
|
XP_011514832.1:n.1695-3880T>G
|
|
|
XR_242190.1:n.1845T>G
|
|
|
|
XR_927520.1:n.1845T>G
|
|
|
|
XR_927521.1:n.1845T>G
|
|
|
|
XR_927522.1:n.1703-3880T>G
|
|
|
|
XR_927523.1:n.1703-3880T>G
|
|
|
|
NM_001354609.1:c.1837T>G
|
NP_001341538.1:p.Leu613Val
|
|
|
NM_004333.5:c.1837T>G
|
NP_004324.2:p.Leu613Val
|
|
|
NR_148928.1:n.2935T>G
|
|
|
|
XM_017012558.1:c.1957T>G
|
XP_016868047.1:p.Leu653Val
|
|
|
XM_017012559.1:c.1957T>G
|
XP_016868048.1:p.Leu653Val
|
|
|
XR_001744857.1:n.1965T>G
|
|
|
|
XR_001744858.1:n.1823-3880T>G
|
|
|
|
NM_001354609.2:c.1837T>G
|
NP_001341538.1:p.Leu613Val
|
|
|
NM_001374244.1:c.1957T>G
|
NP_001361173.1:p.Leu653Val
|
|
|
NM_001374258.1:c.1957T>G
MANE Plus Clinical
|
NP_001361187.1:p.Leu653Val
|
|
|
NM_004333.6:c.1837T>G
MANE Select
|
NP_004324.2:p.Leu613Val
|
|
|
NM_001378467.1:c.1846T>G
|
NP_001365396.1:p.Leu616Val
|
|
|
NM_001378468.1:c.1837T>G
|
NP_001365397.1:p.Leu613Val
|
|
|
NM_001378469.1:c.1771T>G
|
NP_001365398.1:p.Leu591Val
|
|
|
NM_001378470.1:c.1735T>G
|
NP_001365399.1:p.Leu579Val
|
|
|
NM_001378471.1:c.1726T>G
|
NP_001365400.1:p.Leu576Val
|
|
|
NM_001378472.1:c.1681T>G
|
NP_001365401.1:p.Leu561Val
|
|
|
NM_001378473.1:c.1681T>G
|
NP_001365402.1:p.Leu561Val
|
|
|
NM_001378474.1:c.1837T>G
|
NP_001365403.1:p.Leu613Val
|
|
|
NM_001378475.1:c.1573T>G
|
NP_001365404.1:p.Leu525Val
|
|
