ENST00000367990.7:c.258C>T
MANE Select
|
ENSP00000356969.3:p.Phe86=
|
|
ENST00000463273.5:c.258C>T
|
ENSP00000476740.1:p.Phe86=
|
|
ENST00000463812.1:c.114C>T
|
ENSP00000476890.1:p.Phe38=
|
|
ENST00000464492.5:c.357C>T
|
ENSP00000476911.1:p.Phe119=
|
|
ENST00000468465.5:c.114C>T
|
ENSP00000476662.1:p.Phe38=
|
|
ENST00000470459.6:c.204C>T
|
ENSP00000477031.1:p.Phe68=
|
|
ENST00000481413.1:n.769C>T
|
|
|
ENST00000481511.5:c.*255C>T
|
ENSP00000477054.1:n.*255C>T
|
|
ENST00000491350.1:c.*41C>T
|
ENSP00000477353.1:n.*41C>T
|
|
NM_001643.1:c.258C>T
|
NP_001634.1:p.Phe86=
|
|
NM_001643.2:c.258C>T
MANE Select
|
NP_001634.1:p.Phe86=
|
|