ENST00000249806.11:c.807C>T
MANE Select
|
ENSP00000249806.5:p.Thr269=
|
|
ENST00000562767.2:c.84-10641C>T
|
ENSP00000456336.1:n.84-10641C>T
|
|
ENST00000565471.6:c.348C>T
|
ENSP00000457384.1:p.Thr116=
|
|
ENST00000635747.1:c.*710C>T
|
ENSP00000490627.1:n.*710C>T
|
|
ENST00000636212.1:c.*477C>T
|
ENSP00000489851.1:n.*477C>T
|
|
ENST00000636674.1:n.1909C>T
|
|
|
ENST00000636964.1:n.2335C>T
|
|
|
ENST00000637054.1:c.198+10267C>T
|
ENSP00000490807.1:n.198+10267C>T
|
|
ENST00000637329.1:c.776C>T
|
|
|
ENST00000637450.1:c.*461C>T
|
ENSP00000490204.1:n.*461C>T
|
|
ENST00000637494.1:c.519C>T
|
ENSP00000490057.1:p.Thr173=
|
|
ENST00000637667.1:c.708C>T
|
ENSP00000489843.1:p.Thr236=
|
|
ENST00000637823.1:c.632C>T
|
|
|
ENST00000637888.1:c.198+10267C>T
|
ENSP00000490546.1:n.198+10267C>T
|
|
ENST00000638076.1:c.*410C>T
|
ENSP00000490373.1:n.*410C>T
|
|
ENST00000638144.1:n.450C>T
|
|
|
ENST00000646164.1:c.39-8588C>T
|
|
|
ENST00000249806.9:c.807C>T
|
ENSP00000249806.5:p.Thr269=
|
|
ENST00000538696.5:c.903C>T
|
ENSP00000445770.1:p.Thr301=
|
|
ENST00000562767.1:c.84-10641C>T
|
ENSP00000456336.1:n.84-10641C>T
|
|
ENST00000565471.5:c.348C>T
|
ENSP00000457384.1:p.Thr116=
|
|
ENST00000566347.5:c.618C>T
|
ENSP00000457783.1:p.Thr206=
|
|
ENST00000567060.5:c.*205C>T
|
ENSP00000454818.1:n.*205C>T
|
|
NM_017882.2:c.807C>T
|
NP_060352.1:p.Thr269=
|
|
NM_017882.3:c.807C>T
MANE Select
|
NP_060352.1:p.Thr269=
|
|