ENST00000367990.7:c.263G>C
MANE Select
|
ENSP00000356969.3:p.Ser88Thr
|
|
ENST00000463273.5:c.263G>C
|
ENSP00000476740.1:p.Ser88Thr
|
|
ENST00000463812.1:c.119G>C
|
ENSP00000476890.1:p.Ser40Thr
|
|
ENST00000464492.5:c.362G>C
|
ENSP00000476911.1:p.Ser121Thr
|
|
ENST00000468465.5:c.119G>C
|
ENSP00000476662.1:p.Ser40Thr
|
|
ENST00000470459.6:c.209G>C
|
ENSP00000477031.1:p.Ser70Thr
|
|
ENST00000481413.1:n.774G>C
|
|
|
ENST00000481511.5:c.*260G>C
|
ENSP00000477054.1:n.*260G>C
|
|
ENST00000491350.1:c.*46G>C
|
ENSP00000477353.1:n.*46G>C
|
|
NM_001643.1:c.263G>C
|
NP_001634.1:p.Ser88Thr
|
|
NM_001643.2:c.263G>C
MANE Select
|
NP_001634.1:p.Ser88Thr
|
|