ENST00000367990.7:c.252T>G
MANE Select
|
ENSP00000356969.3:p.Val84=
|
|
ENST00000463273.5:c.252T>G
|
ENSP00000476740.1:p.Val84=
|
|
ENST00000463812.1:c.108T>G
|
ENSP00000476890.1:p.Val36=
|
|
ENST00000464492.5:c.351T>G
|
ENSP00000476911.1:p.Val117=
|
|
ENST00000468465.5:c.108T>G
|
ENSP00000476662.1:p.Val36=
|
|
ENST00000470459.6:c.201-3T>G
|
ENSP00000477031.1:n.201-3T>G
|
|
ENST00000481413.1:n.763T>G
|
|
|
ENST00000481511.5:c.*249T>G
|
ENSP00000477054.1:n.*249T>G
|
|
ENST00000491350.1:c.*35T>G
|
ENSP00000477353.1:n.*35T>G
|
|
NM_001643.1:c.252T>G
|
NP_001634.1:p.Val84=
|
|
NM_001643.2:c.252T>G
MANE Select
|
NP_001634.1:p.Val84=
|
|