ENST00000249806.11:c.569T>A
MANE Select
|
ENSP00000249806.5:p.Phe190Tyr
|
|
ENST00000562767.2:c.84-12105T>A
|
ENSP00000456336.1:n.84-12105T>A
|
|
ENST00000563917.2:n.411T>A
|
|
|
ENST00000565471.6:c.110T>A
|
ENSP00000457384.1:p.Phe37Tyr
|
|
ENST00000635747.1:c.*472T>A
|
ENSP00000490627.1:n.*472T>A
|
|
ENST00000636212.1:c.*239T>A
|
ENSP00000489851.1:n.*239T>A
|
|
ENST00000636314.1:c.265T>A
|
ENSP00000490295.1:p.Ser89Thr
|
|
ENST00000636674.1:n.1671T>A
|
|
|
ENST00000636964.1:n.2097T>A
|
|
|
ENST00000637054.1:c.198+8803T>A
|
ENSP00000490807.1:n.198+8803T>A
|
|
ENST00000637223.1:c.*283T>A
|
ENSP00000490010.1:n.*283T>A
|
|
ENST00000637329.1:c.538T>A
|
|
|
ENST00000637450.1:c.*223T>A
|
ENSP00000490204.1:n.*223T>A
|
|
ENST00000637494.1:c.281T>A
|
ENSP00000490057.1:p.Phe94Tyr
|
|
ENST00000637667.1:c.470T>A
|
ENSP00000489843.1:p.Phe157Tyr
|
|
ENST00000637823.1:c.394T>A
|
|
|
ENST00000637888.1:c.198+8803T>A
|
ENSP00000490546.1:n.198+8803T>A
|
|
ENST00000638076.1:c.*172T>A
|
ENSP00000490373.1:n.*172T>A
|
|
ENST00000638144.1:n.212T>A
|
|
|
ENST00000646164.1:c.38+8803T>A
|
|
|
ENST00000249806.9:c.569T>A
|
ENSP00000249806.5:p.Phe190Tyr
|
|
ENST00000538696.5:c.665T>A
|
ENSP00000445770.1:p.Phe222Tyr
|
|
ENST00000562767.1:c.84-12105T>A
|
ENSP00000456336.1:n.84-12105T>A
|
|
ENST00000563917.1:n.469T>A
|
|
|
ENST00000564752.1:c.595T>A
|
ENSP00000457822.1:p.Ser199Thr
|
|
ENST00000565471.5:c.110T>A
|
ENSP00000457384.1:p.Phe37Tyr
|
|
ENST00000566347.5:c.380T>A
|
ENSP00000457783.1:p.Phe127Tyr
|
|
ENST00000567060.5:c.298-13T>A
|
ENSP00000454818.1:n.298-13T>A
|
|
NM_017882.2:c.569T>A
|
NP_060352.1:p.Phe190Tyr
|
|
XR_931861.1:n.791T>A
|
|
|
NM_017882.3:c.569T>A
MANE Select
|
NP_060352.1:p.Phe190Tyr
|
|