ENST00000376091.8:c.1286A>T
MANE Select
|
ENSP00000365259.3:p.Glu429Val
|
|
ENST00000642383.1:c.536A>T
|
ENSP00000496353.1:p.Glu179Val
|
|
ENST00000642885.1:c.1076A>T
|
ENSP00000496632.1:p.Glu359Val
|
|
ENST00000643129.1:c.1573A>T
|
|
|
ENST00000646398.1:c.*461A>T
|
ENSP00000495122.1:n.*461A>T
|
|
ENST00000307367.2:c.1076A>T
|
ENSP00000304257.2:p.Glu359Val
|
|
ENST00000376088.7:c.1286A>T
|
ENSP00000365256.3:p.Glu429Val
|
|
ENST00000376091.7:c.1286A>T
|
ENSP00000365259.3:p.Glu429Val
|
|
ENST00000376108.7:c.1076A>T
|
ENSP00000365276.3:p.Glu359Val
|
|
NM_000084.4:c.1076A>T
|
NP_000075.1:p.Glu359Val
|
|
NM_001127898.3:c.1286A>T
|
NP_001121370.1:p.Glu429Val
|
|
NM_001127899.3:c.1286A>T
|
NP_001121371.1:p.Glu429Val
|
|
NM_001282163.1:c.1136A>T
|
NP_001269092.1:p.Glu379Val
|
|
XM_011543888.1:c.1286A>T
|
XP_011542190.1:p.Glu429Val
|
|
XM_011543889.1:c.1076A>T
|
XP_011542191.1:p.Glu359Val
|
|
XM_017029257.1:c.1298A>T
|
XP_016884746.1:p.Glu433Val
|
|
XM_017029258.1:c.1298A>T
|
XP_016884747.1:p.Glu433Val
|
|
NM_001127898.4:c.1286A>T
MANE Select
|
NP_001121370.1:p.Glu429Val
|
|
NM_000084.5:c.1076A>T
|
NP_000075.1:p.Glu359Val
|
|
NM_001127899.4:c.1286A>T
|
NP_001121371.1:p.Glu429Val
|
|
NM_001282163.2:c.1136A>T
|
NP_001269092.1:p.Glu379Val
|
|