|
ENST00000473665.2:n.5938A>T
|
|
|
|
ENST00000482662.2:n.4345A>T
|
|
|
|
ENST00000685865.1:n.2297A>T
|
|
|
|
ENST00000687250.1:n.1997A>T
|
|
|
|
ENST00000687995.1:n.1812A>T
|
|
|
|
ENST00000688205.1:c.*1053A>T
|
ENSP00000509673.1:n.*1053A>T
|
|
|
ENST00000688788.1:n.1699A>T
|
|
|
|
ENST00000689276.1:c.1391A>T
|
ENSP00000510012.1:p.Asp464Val
|
|
|
ENST00000689576.1:c.*79A>T
|
ENSP00000508712.1:n.*79A>T
|
|
|
ENST00000690108.1:c.*1116A>T
|
ENSP00000510617.1:n.*1116A>T
|
|
|
ENST00000690468.1:c.*12A>T
|
ENSP00000509078.1:n.*12A>T
|
|
|
ENST00000690595.1:c.785A>T
|
ENSP00000508979.1:p.Asp262Val
|
|
|
ENST00000691348.1:c.*12A>T
|
ENSP00000509369.1:n.*12A>T
|
|
|
ENST00000691410.1:c.*1037A>T
|
ENSP00000508479.1:n.*1037A>T
|
|
|
ENST00000693287.1:c.776A>T
|
ENSP00000510264.1:p.Asp259Val
|
|
|
ENST00000693681.1:c.773A>T
|
ENSP00000510789.1:p.Asp258Val
|
|
|
ENST00000233838.9:c.1460A>T
MANE Select
|
ENSP00000233838.3:p.Asp487Val
|
|
|
ENST00000233838.8:c.1460A>T
|
ENSP00000233838.3:p.Asp487Val
|
|
|
ENST00000430215.7:c.1289A>T
|
ENSP00000408045.3:p.Asp430Val
|
|
|
ENST00000465637.5:n.179-3957A>T
|
|
|
|
NM_000821.5:c.1460A>T
|
NP_000812.2:p.Asp487Val
|
|
|
NM_000821.6:c.1460A>T
|
NP_000812.2:p.Asp487Val
|
|
|
NM_001142269.2:c.1289A>T
|
NP_001135741.1:p.Asp430Val
|
|
|
NM_001142269.3:c.1289A>T
|
NP_001135741.1:p.Asp430Val
|
|
|
XM_005264259.3:c.1460A>T
|
XP_005264316.1:p.Asp487Val
|
|
|
XM_011532764.1:c.638A>T
|
XP_011531066.1:p.Asp213Val
|
|
|
XM_011532765.1:c.638A>T
|
XP_011531067.1:p.Asp213Val
|
|
|
XR_939677.1:n.1373A>T
|
|
|
|
XM_005264259.5:c.1460A>T
|
XP_005264316.1:p.Asp487Val
|
|
|
XM_011532764.3:c.638A>T
|
XP_011531066.1:p.Asp213Val
|
|
|
XM_011532765.3:c.638A>T
|
XP_011531067.1:p.Asp213Val
|
|
|
XM_017003803.2:c.1289A>T
|
XP_016859292.1:p.Asp430Val
|
|
|
XR_001738703.2:n.1373A>T
|
|
|
|
NM_000821.7:c.1460A>T
MANE Select
|
NP_000812.2:p.Asp487Val
|
|
|
NM_001142269.4:c.1289A>T
|
NP_001135741.1:p.Asp430Val
|
|
