ENST00000252490.7:c.192G>T
(APOC2)
MANE Select
|
ENSP00000252490.5:p.Leu64=
|
|
ENST00000252490.5:c.192G>T
(APOC4-APOC2)
|
ENSP00000252490.4:p.Leu64=
|
|
ENST00000585685.5:c.*975G>T
(APOC4-APOC2)
|
ENSP00000467185.1:n.*975G>T
|
|
ENST00000585786.1:c.192G>T
(APOC2)
|
ENSP00000465001.1:p.Leu64=
|
|
ENST00000589057.5:c.423G>T
(APOC4-APOC2)
|
ENSP00000468139.1:p.Leu141=
|
|
ENST00000590360.2:c.192G>T
(APOC2)
|
ENSP00000466775.1:p.Leu64=
|
|
ENST00000591597.5:c.173+19G>T
(APOC2)
|
ENSP00000476835.1:n.173+19G>T
|
|
ENST00000592257.5:c.130G>T
(APOC2)
|
ENSP00000477261.1:p.Ala44Ser
|
|
NM_000483.4:c.192G>T
(APOC2)
|
NP_000474.2:p.Leu64=
|
|
NR_037932.1:n.1399G>T
(APOC4-APOC2)
|
|
|
NM_000483.5:c.192G>T
(APOC2)
MANE Select
|
NP_000474.2:p.Leu64=
|
|