ENST00000367990.7:c.266A>T
MANE Select
|
ENSP00000356969.3:p.Tyr89Phe
|
|
ENST00000463273.5:c.266A>T
|
ENSP00000476740.1:p.Tyr89Phe
|
|
ENST00000463812.1:c.122A>T
|
ENSP00000476890.1:p.Tyr41Phe
|
|
ENST00000464492.5:c.365A>T
|
ENSP00000476911.1:p.Tyr122Phe
|
|
ENST00000468465.5:c.122A>T
|
ENSP00000476662.1:p.Tyr41Phe
|
|
ENST00000470459.6:c.212A>T
|
ENSP00000477031.1:p.Tyr71Phe
|
|
ENST00000481413.1:n.777A>T
|
|
|
ENST00000481511.5:c.*263A>T
|
ENSP00000477054.1:n.*263A>T
|
|
ENST00000491350.1:c.*49A>T
|
ENSP00000477353.1:n.*49A>T
|
|
NM_001643.1:c.266A>T
|
NP_001634.1:p.Tyr89Phe
|
|
NM_001643.2:c.266A>T
MANE Select
|
NP_001634.1:p.Tyr89Phe
|
|