ENST00000252490.7:c.295G>T
(APOC2)
MANE Select
|
ENSP00000252490.5:p.Gly99Ter
|
|
ENST00000252490.5:c.295G>T
(APOC4-APOC2)
|
ENSP00000252490.4:p.Gly99Ter
|
|
ENST00000585685.5:c.*1078G>T
(APOC4-APOC2)
|
ENSP00000467185.1:n.*1078G>T
|
|
ENST00000585786.1:c.*374G>T
(APOC2)
|
ENSP00000465001.1:n.*374G>T
|
|
ENST00000589057.5:c.526G>T
(APOC4-APOC2)
|
ENSP00000468139.1:p.Gly176Ter
|
|
ENST00000590360.2:c.295G>T
(APOC2)
|
ENSP00000466775.1:p.Gly99Ter
|
|
ENST00000591597.5:c.253G>T
(APOC2)
|
ENSP00000476835.1:p.Gly85Ter
|
|
ENST00000592257.5:c.*89G>T
(APOC2)
|
ENSP00000477261.1:n.*89G>T
|
|
NM_000483.4:c.295G>T
(APOC2)
|
NP_000474.2:p.Gly99Ter
|
|
NR_037932.1:n.1502G>T
(APOC4-APOC2)
|
|
|
NM_000483.5:c.295G>T
(APOC2)
MANE Select
|
NP_000474.2:p.Gly99Ter
|
|