ENST00000336418.9:c.*4490G>C
(AP3S2)
MANE Select
|
ENSP00000338777.4:n.*4490G>C
|
|
ENST00000336418.8:c.*4490G>C
(AP3S2)
|
ENSP00000338777.4:n.*4490G>C
|
|
NM_001199058.1:c.*4490G>C
(ARPIN-AP3S2)
|
NP_001185987.1:n.*4490G>C
|
|
NM_005829.4:c.*4490G>C
(AP3S2)
|
NP_005820.1:n.*4490G>C
|
|
NR_023361.1:n.5627G>C
(AP3S2)
|
|
|
NR_037582.1:n.5504G>C
(AP3S2)
|
|
|
NM_005829.5:c.*4490G>C
(AP3S2)
MANE Select
|
NP_005820.1:n.*4490G>C
|
|
NM_001199058.2:c.*4490G>C
(ARPIN-AP3S2)
|
NP_001185987.1:n.*4490G>C
|
|
NR_023361.2:n.5236G>C
(AP3S2)
|
|
|
NR_037582.2:n.5113G>C
(AP3S2)
|
|
|