ENST00000249806.11:c.709A>T
MANE Select
|
ENSP00000249806.5:p.Thr237Ser
|
|
ENST00000562767.2:c.84-10739A>T
|
ENSP00000456336.1:n.84-10739A>T
|
|
ENST00000563917.2:n.551A>T
|
|
|
ENST00000565471.6:c.250A>T
|
ENSP00000457384.1:p.Thr84Ser
|
|
ENST00000635747.1:c.*612A>T
|
ENSP00000490627.1:n.*612A>T
|
|
ENST00000636212.1:c.*379A>T
|
ENSP00000489851.1:n.*379A>T
|
|
ENST00000636674.1:n.1811A>T
|
|
|
ENST00000636964.1:n.2237A>T
|
|
|
ENST00000637054.1:c.198+10169A>T
|
ENSP00000490807.1:n.198+10169A>T
|
|
ENST00000637329.1:c.678A>T
|
|
|
ENST00000637450.1:c.*363A>T
|
ENSP00000490204.1:n.*363A>T
|
|
ENST00000637494.1:c.421A>T
|
ENSP00000490057.1:p.Thr141Ser
|
|
ENST00000637667.1:c.610A>T
|
ENSP00000489843.1:p.Thr204Ser
|
|
ENST00000637823.1:c.534A>T
|
|
|
ENST00000637888.1:c.198+10169A>T
|
ENSP00000490546.1:n.198+10169A>T
|
|
ENST00000638076.1:c.*312A>T
|
ENSP00000490373.1:n.*312A>T
|
|
ENST00000638144.1:n.352A>T
|
|
|
ENST00000646164.1:c.39-8686A>T
|
|
|
ENST00000249806.9:c.709A>T
|
ENSP00000249806.5:p.Thr237Ser
|
|
ENST00000538696.5:c.805A>T
|
ENSP00000445770.1:p.Thr269Ser
|
|
ENST00000562767.1:c.84-10739A>T
|
ENSP00000456336.1:n.84-10739A>T
|
|
ENST00000564752.1:c.*93A>T
|
ENSP00000457822.1:n.*93A>T
|
|
ENST00000565471.5:c.250A>T
|
ENSP00000457384.1:p.Thr84Ser
|
|
ENST00000566347.5:c.520A>T
|
ENSP00000457783.1:p.Thr174Ser
|
|
ENST00000567060.5:c.*107A>T
|
ENSP00000454818.1:n.*107A>T
|
|
NM_017882.2:c.709A>T
|
NP_060352.1:p.Thr237Ser
|
|
NM_017882.3:c.709A>T
MANE Select
|
NP_060352.1:p.Thr237Ser
|
|