ENST00000252490.7:c.271G>C
(APOC2)
MANE Select
|
ENSP00000252490.5:p.Asp91His
|
|
ENST00000252490.5:c.271G>C
(APOC4-APOC2)
|
ENSP00000252490.4:p.Asp91His
|
|
ENST00000585685.5:c.*1054G>C
(APOC4-APOC2)
|
ENSP00000467185.1:n.*1054G>C
|
|
ENST00000585786.1:c.*350G>C
(APOC2)
|
ENSP00000465001.1:n.*350G>C
|
|
ENST00000589057.5:c.502G>C
(APOC4-APOC2)
|
ENSP00000468139.1:p.Asp168His
|
|
ENST00000590360.2:c.271G>C
(APOC2)
|
ENSP00000466775.1:p.Asp91His
|
|
ENST00000591597.5:c.229G>C
(APOC2)
|
ENSP00000476835.1:p.Asp77His
|
|
ENST00000592257.5:c.*65G>C
(APOC2)
|
ENSP00000477261.1:n.*65G>C
|
|
NM_000483.4:c.271G>C
(APOC2)
|
NP_000474.2:p.Asp91His
|
|
NR_037932.1:n.1478G>C
(APOC4-APOC2)
|
|
|
NM_000483.5:c.271G>C
(APOC2)
MANE Select
|
NP_000474.2:p.Asp91His
|
|