ENST00000332351.9:c.1343T>G
|
ENSP00000331327.5:p.Phe448Cys
|
|
ENST00000379077.9:c.*578T>G
|
ENSP00000368368.5:n.*578T>G
|
|
ENST00000379079.8:c.743T>G
|
ENSP00000368370.2:p.Phe248Cys
|
|
ENST00000448076.9:c.1394T>G
|
ENSP00000413452.5:p.Phe465Cys
|
|
ENST00000452863.10:c.1394T>G
MANE Select
|
ENSP00000415516.5:p.Phe465Cys
|
|
ENST00000526685.2:n.848T>G
|
|
|
ENST00000639563.3:c.1343T>G
|
ENSP00000492269.3:p.Phe448Cys
|
|
ENST00000639907.2:n.537T>G
|
|
|
ENST00000640146.2:c.719T>G
|
ENSP00000491984.2:p.Phe240Cys
|
|
ENST00000650745.1:n.1204T>G
|
|
|
ENST00000650861.1:n.1975T>G
|
|
|
ENST00000650986.1:n.57T>G
|
|
|
ENST00000651459.1:c.165T>G
|
|
|
ENST00000651533.1:n.440T>G
|
|
|
ENST00000651668.1:n.331T>G
|
|
|
ENST00000651794.1:n.1237T>G
|
|
|
ENST00000651819.1:n.319T>G
|
|
|
ENST00000652579.1:n.654T>G
|
|
|
ENST00000652724.1:n.584T>G
|
|
|
ENST00000332351.7:c.1379T>G
|
ENSP00000331327.3:p.Phe460Cys
|
|
ENST00000379077.7:c.*578T>G
|
ENSP00000368368.3:n.*578T>G
|
|
ENST00000379079.6:c.743T>G
|
ENSP00000368370.2:p.Phe248Cys
|
|
ENST00000448076.7:c.1379T>G
|
ENSP00000413452.3:p.Phe460Cys
|
|
ENST00000452863.7:c.1328T>G
|
ENSP00000415516.3:p.Phe443Cys
|
|
ENST00000527882.5:c.360T>G
|
|
|
ENST00000530998.5:c.692T>G
|
ENSP00000435307.1:p.Phe231Cys
|
|
NM_000378.4:c.1328T>G
|
NP_000369.3:p.Phe443Cys
|
|
NM_001198551.1:c.743T>G , LRG_525t2:c.743T>G
|
NP_001185480.1:p.Phe248Cys
|
|
NM_001198552.1:c.692T>G
|
NP_001185481.1:p.Phe231Cys
|
|
NM_024424.3:c.1379T>G
|
NP_077742.2:p.Phe460Cys
|
|
NM_024426.4:c.1379T>G
|
NP_077744.3:p.Phe460Cys
|
|
NM_000378.5:c.1343T>G
|
NP_000369.4:p.Phe448Cys
|
|
NM_024424.4:c.1394T>G
|
NP_077742.3:p.Phe465Cys
|
|
NM_024426.5:c.1394T>G
|
NP_077744.4:p.Phe465Cys
|
|
NM_001367854.1:c.206T>G
|
NP_001354783.1:p.Phe69Cys
|
|
NR_160306.1:n.1726T>G
|
|
|
NM_000378.6:c.1343T>G
|
NP_000369.4:p.Phe448Cys
|
|
NM_001198552.2:c.692T>G
|
NP_001185481.1:p.Phe231Cys
|
|
NM_024424.5:c.1394T>G
|
NP_077742.3:p.Phe465Cys
|
|
NM_024426.6:c.1394T>G
MANE Select
|
NP_077744.4:p.Phe465Cys
|
|