ENST00000367990.7:c.*12C>G
MANE Select
|
ENSP00000356969.3:n.*12C>G
|
|
ENST00000463812.1:c.*12C>G
|
ENSP00000476890.1:n.*12C>G
|
|
ENST00000464492.5:c.*12C>G
|
ENSP00000476911.1:n.*12C>G
|
|
ENST00000468465.5:c.*12C>G
|
ENSP00000476662.1:n.*12C>G
|
|
ENST00000470459.6:c.*12C>G
|
ENSP00000477031.1:n.*12C>G
|
|
ENST00000481413.1:n.826C>G
|
|
|
ENST00000481511.5:c.*312C>G
|
ENSP00000477054.1:n.*312C>G
|
|
ENST00000491350.1:c.*98C>G
|
ENSP00000477353.1:n.*98C>G
|
|
NM_001643.1:c.*12C>G
|
NP_001634.1:n.*12C>G
|
|
NM_001643.2:c.*12C>G
MANE Select
|
NP_001634.1:n.*12C>G
|
|