ENST00000698724.1:n.1879T>A
|
|
|
ENST00000698725.1:n.1632T>A
|
|
|
ENST00000698726.1:n.3192T>A
|
|
|
ENST00000698727.1:n.2925T>A
|
|
|
ENST00000698728.1:n.3541T>A
|
|
|
ENST00000698729.1:n.4989T>A
|
|
|
ENST00000698730.1:n.5087T>A
|
|
|
ENST00000698731.1:c.3821T>A
|
ENSP00000513898.1:p.Phe1274Tyr
|
|
ENST00000698732.1:c.*2651T>A
|
ENSP00000513899.1:n.*2651T>A
|
|
ENST00000698733.1:c.*3149T>A
|
ENSP00000513900.1:n.*3149T>A
|
|
ENST00000698734.1:c.*2135T>A
|
ENSP00000513901.1:n.*2135T>A
|
|
ENST00000698735.1:n.4313T>A
|
|
|
ENST00000698736.1:n.4726T>A
|
|
|
ENST00000698737.1:n.4077T>A
|
|
|
ENST00000372371.8:c.3962T>A
MANE Select
|
ENSP00000361446.3:p.Phe1321Tyr
|
|
ENST00000372371.7:c.3962T>A
|
ENSP00000361446.3:p.Phe1321Tyr
|
|
ENST00000616246.4:c.410T>A
|
ENSP00000483738.1:p.Phe137Tyr
|
|
NM_007055.3:c.3962T>A
|
NP_008986.2:p.Phe1321Tyr
|
|
NM_007055.4:c.3962T>A
MANE Select
|
NP_008986.2:p.Phe1321Tyr
|
|