NM_001643.1:c.186-4C>T
|
NP_001634.1:p.=
|
|
NM_001643.2:c.186-4C>T
MANE Select
|
NP_001634.1:p.=
|
|
ENST00000367990.7:c.186-4C>T
|
ENSP00000356969.3:p.=
|
|
ENST00000463273.5:c.186-4C>T
|
ENSP00000476740.1:p.=
|
|
ENST00000463812.1:c.42-4C>T
|
ENSP00000476890.1:p.=
|
|
ENST00000464492.5:c.285-4C>T
|
ENSP00000476911.1:p.=
|
|
ENST00000468465.5:c.42-4C>T
|
ENSP00000476662.1:p.=
|
|
ENST00000469730.2:c.186-4C>T
|
ENSP00000476605.1:p.=
|
|
ENST00000470459.6:c.186-4C>T
|
ENSP00000477031.1:p.=
|
|
ENST00000481413.1:n.697-4C>T
|
|
|
ENST00000481511.5:c.*183-4C>T
|
ENSP00000477054.1:p.=
|
|
ENST00000491350.1:c.53-4C>T
|
ENSP00000477353.1:p.=
|
|