|
ENST00000332351.9:c.983A>T
|
ENSP00000331327.5:p.Glu328Val
|
|
|
ENST00000379077.9:c.*218A>T
|
ENSP00000368368.5:n.*218A>T
|
|
|
ENST00000379079.8:c.383A>T
|
ENSP00000368370.2:p.Glu128Val
|
|
|
ENST00000448076.9:c.1034A>T
|
ENSP00000413452.5:p.Glu345Val
|
|
|
ENST00000452863.10:c.1034A>T
MANE Select
|
ENSP00000415516.5:p.Glu345Val
|
|
|
ENST00000526685.2:n.488A>T
|
|
|
|
ENST00000639563.3:c.983A>T
|
ENSP00000492269.3:p.Glu328Val
|
|
|
ENST00000639907.2:n.177A>T
|
|
|
|
ENST00000640146.2:c.359A>T
|
ENSP00000491984.2:p.Glu120Val
|
|
|
ENST00000651794.1:n.777A>T
|
|
|
|
ENST00000652579.1:n.194A>T
|
|
|
|
ENST00000652724.1:n.224A>T
|
|
|
|
ENST00000332351.7:c.1019A>T
|
ENSP00000331327.3:p.Glu340Val
|
|
|
ENST00000379077.7:c.*218A>T
|
ENSP00000368368.3:n.*218A>T
|
|
|
ENST00000379079.6:c.383A>T
|
ENSP00000368370.2:p.Glu128Val
|
|
|
ENST00000448076.7:c.1019A>T
|
ENSP00000413452.3:p.Glu340Val
|
|
|
ENST00000452863.7:c.968A>T
|
ENSP00000415516.3:p.Glu323Val
|
|
|
ENST00000526685.1:c.-155A>T
|
ENSP00000436292.1:n.-155A>T
|
|
|
ENST00000527775.1:c.272A>T
|
ENSP00000435351.1:p.Glu91Val
|
|
|
ENST00000527882.5:c.90A>T
|
|
|
|
ENST00000530998.5:c.332A>T
|
ENSP00000435307.1:p.Glu111Val
|
|
|
NM_000378.4:c.968A>T
|
NP_000369.3:p.Glu323Val
|
|
|
NM_001198551.1:c.383A>T , LRG_525t2:c.383A>T
|
NP_001185480.1:p.Glu128Val
|
|
|
NM_001198552.1:c.332A>T
|
NP_001185481.1:p.Glu111Val
|
|
|
NM_024424.3:c.1019A>T
|
NP_077742.2:p.Glu340Val
|
|
|
NM_024426.4:c.1019A>T
|
NP_077744.3:p.Glu340Val
|
|
|
NM_000378.5:c.983A>T
|
NP_000369.4:p.Glu328Val
|
|
|
NM_024424.4:c.1034A>T
|
NP_077742.3:p.Glu345Val
|
|
|
NM_024426.5:c.1034A>T
|
NP_077744.4:p.Glu345Val
|
|
|
NM_001367854.1:c.-155A>T
|
NP_001354783.1:n.-155A>T
|
|
|
NR_160306.1:n.1366A>T
|
|
|
|
NM_000378.6:c.983A>T
|
NP_000369.4:p.Glu328Val
|
|
|
NM_001198552.2:c.332A>T
|
NP_001185481.1:p.Glu111Val
|
|
|
NM_024424.5:c.1034A>T
|
NP_077742.3:p.Glu345Val
|
|
|
NM_024426.6:c.1034A>T
MANE Select
|
NP_077744.4:p.Glu345Val
|
|
