|
ENST00000332351.9:c.1315T=
|
ENSP00000331327.5:p.Phe439=
|
|
|
ENST00000379077.9:c.*550T=
|
ENSP00000368368.5:n.*550T=
|
|
|
ENST00000379079.8:c.715T=
|
ENSP00000368370.2:p.Phe239=
|
|
|
ENST00000448076.9:c.1366T=
|
ENSP00000413452.5:p.Phe456=
|
|
|
ENST00000452863.10:c.1366T=
MANE Select
|
ENSP00000415516.5:p.Phe456=
|
|
|
ENST00000526685.2:n.820T=
|
|
|
|
ENST00000639563.3:c.1315T=
|
ENSP00000492269.3:p.Phe439=
|
|
|
ENST00000639907.2:n.509T=
|
|
|
|
ENST00000640146.2:c.691T=
|
ENSP00000491984.2:p.Phe231=
|
|
|
ENST00000650745.1:n.1176T=
|
|
|
|
ENST00000650861.1:n.1947T=
|
|
|
|
ENST00000650986.1:n.29T=
|
|
|
|
ENST00000651459.1:c.137T=
|
|
|
|
ENST00000651533.1:n.412T=
|
|
|
|
ENST00000651668.1:n.303T=
|
|
|
|
ENST00000651794.1:n.1209T=
|
|
|
|
ENST00000651819.1:n.291T=
|
|
|
|
ENST00000652579.1:n.626T=
|
|
|
|
ENST00000652724.1:n.556T=
|
|
|
|
ENST00000332351.7:c.1351T=
|
ENSP00000331327.3:p.Phe451=
|
|
|
ENST00000379077.7:c.*550T=
|
ENSP00000368368.3:n.*550T=
|
|
|
ENST00000379079.6:c.715T=
|
ENSP00000368370.2:p.Phe239=
|
|
|
ENST00000448076.7:c.1351T=
|
ENSP00000413452.3:p.Phe451=
|
|
|
ENST00000452863.7:c.1300T=
|
ENSP00000415516.3:p.Phe434=
|
|
|
ENST00000527882.5:c.332T=
|
|
|
|
ENST00000530998.5:c.664T=
|
ENSP00000435307.1:p.Phe222=
|
|
|
NM_000378.4:c.1300T=
|
NP_000369.3:p.Phe434=
|
|
|
NM_001198551.1:c.715T= , LRG_525t2:c.715T=
|
NP_001185480.1:p.Phe239=
|
|
|
NM_001198552.1:c.664T=
|
NP_001185481.1:p.Phe222=
|
|
|
NM_024424.3:c.1351T=
|
NP_077742.2:p.Phe451=
|
|
|
NM_024426.4:c.1351T=
|
NP_077744.3:p.Phe451=
|
|
|
NM_000378.5:c.1315T=
|
NP_000369.4:p.Phe439=
|
|
|
NM_024424.4:c.1366T=
|
NP_077742.3:p.Phe456=
|
|
|
NM_024426.5:c.1366T=
|
NP_077744.4:p.Phe456=
|
|
|
NM_001367854.1:c.178T=
|
NP_001354783.1:p.Phe60=
|
|
|
NR_160306.1:n.1698T=
|
|
|
|
NM_000378.6:c.1315T=
|
NP_000369.4:p.Phe439=
|
|
|
NM_001198552.2:c.664T=
|
NP_001185481.1:p.Phe222=
|
|
|
NM_024424.5:c.1366T=
|
NP_077742.3:p.Phe456=
|
|
|
NM_024426.6:c.1366T=
MANE Select
|
NP_077744.4:p.Phe456=
|
|
