ENST00000332351.9:c.1238T>A
|
ENSP00000331327.5:p.Phe413Tyr
|
|
ENST00000379077.9:c.*473T>A
|
ENSP00000368368.5:n.*473T>A
|
|
ENST00000379079.8:c.638T>A
|
ENSP00000368370.2:p.Phe213Tyr
|
|
ENST00000448076.9:c.1289T>A
|
ENSP00000413452.5:p.Phe430Tyr
|
|
ENST00000452863.10:c.1289T>A
MANE Select
|
ENSP00000415516.5:p.Phe430Tyr
|
|
ENST00000526685.2:n.743T>A
|
|
|
ENST00000639563.3:c.1238T>A
|
ENSP00000492269.3:p.Phe413Tyr
|
|
ENST00000639907.2:n.432T>A
|
|
|
ENST00000640146.2:c.614T>A
|
ENSP00000491984.2:p.Phe205Tyr
|
|
ENST00000650745.1:n.498T>A
|
|
|
ENST00000650861.1:n.1870T>A
|
|
|
ENST00000651459.1:c.60T>A
|
|
|
ENST00000651533.1:n.335T>A
|
|
|
ENST00000651668.1:n.226T>A
|
|
|
ENST00000651794.1:n.1132T>A
|
|
|
ENST00000651819.1:n.214T>A
|
|
|
ENST00000652579.1:n.549T>A
|
|
|
ENST00000652724.1:n.479T>A
|
|
|
ENST00000332351.7:c.1274T>A
|
ENSP00000331327.3:p.Phe425Tyr
|
|
ENST00000379077.7:c.*473T>A
|
ENSP00000368368.3:n.*473T>A
|
|
ENST00000379079.6:c.638T>A
|
ENSP00000368370.2:p.Phe213Tyr
|
|
ENST00000448076.7:c.1274T>A
|
ENSP00000413452.3:p.Phe425Tyr
|
|
ENST00000452863.7:c.1223T>A
|
ENSP00000415516.3:p.Phe408Tyr
|
|
ENST00000527882.5:c.321-667T>A
|
|
|
ENST00000530998.5:c.587T>A
|
ENSP00000435307.1:p.Phe196Tyr
|
|
NM_000378.4:c.1223T>A
|
NP_000369.3:p.Phe408Tyr
|
|
NM_001198551.1:c.638T>A , LRG_525t2:c.638T>A
|
NP_001185480.1:p.Phe213Tyr
|
|
NM_001198552.1:c.587T>A
|
NP_001185481.1:p.Phe196Tyr
|
|
NM_024424.3:c.1274T>A
|
NP_077742.2:p.Phe425Tyr
|
|
NM_024426.4:c.1274T>A
|
NP_077744.3:p.Phe425Tyr
|
|
NM_000378.5:c.1238T>A
|
NP_000369.4:p.Phe413Tyr
|
|
NM_024424.4:c.1289T>A
|
NP_077742.3:p.Phe430Tyr
|
|
NM_024426.5:c.1289T>A
|
NP_077744.4:p.Phe430Tyr
|
|
NM_001367854.1:c.101T>A
|
NP_001354783.1:p.Phe34Tyr
|
|
NR_160306.1:n.1621T>A
|
|
|
NM_000378.6:c.1238T>A
|
NP_000369.4:p.Phe413Tyr
|
|
NM_001198552.2:c.587T>A
|
NP_001185481.1:p.Phe196Tyr
|
|
NM_024424.5:c.1289T>A
|
NP_077742.3:p.Phe430Tyr
|
|
NM_024426.6:c.1289T>A
MANE Select
|
NP_077744.4:p.Phe430Tyr
|
|