|
ENST00000261722.8:c.2951G>C
(AP3B2)
|
ENSP00000261722.4:p.Ser984Thr
|
|
|
ENST00000535359.6:c.2990G>C
(AP3B2)
MANE Select
|
ENSP00000440984.1:p.Ser997Thr
|
|
|
ENST00000535385.6:n.3877G>C
(AP3B2)
|
|
|
|
ENST00000537735.2:n.3079G>C
(AP3B2)
|
|
|
|
ENST00000543938.6:n.3577G>C
(AP3B2)
|
|
|
|
ENST00000642989.2:c.3062G>C
(AP3B2)
|
ENSP00000493485.1:p.Ser1021Thr
|
|
|
ENST00000652847.1:c.2933G>C
(AP3B2)
|
ENSP00000499785.1:p.Ser978Thr
|
|
|
ENST00000657321.1:c.*2779G>C
(AP3B2)
|
ENSP00000499716.1:n.*2779G>C
|
|
|
ENST00000660624.1:c.1841G>C
(AP3B2)
|
ENSP00000499379.1:p.Ser614Thr
|
|
|
ENST00000661532.1:c.2222G>C
(AP3B2)
|
|
|
|
ENST00000663651.1:n.3075G>C
(AP3B2)
|
|
|
|
ENST00000666973.1:c.2933G>C
(AP3B2)
|
ENSP00000499288.1:p.Ser978Thr
|
|
|
ENST00000667758.1:c.*3588G>C
(AP3B2)
|
ENSP00000499318.1:n.*3588G>C
|
|
|
ENST00000668385.1:c.*2731G>C
(AP3B2)
|
ENSP00000499544.1:n.*2731G>C
|
|
|
ENST00000668458.1:c.2681G>C
(AP3B2)
|
|
|
|
ENST00000668990.2:c.2933G>C
(AP3B2)
|
ENSP00000499235.1:p.Ser978Thr
|
|
|
ENST00000669930.1:c.2762G>C
(AP3B2)
|
ENSP00000499671.1:p.Ser921Thr
|
|
|
ENST00000679388.1:n.3517G>C
(AP3B2)
|
|
|
|
ENST00000679531.1:n.3780G>C
(AP3B2)
|
|
|
|
ENST00000679891.1:n.1811G>C
(AP3B2)
|
|
|
|
ENST00000679950.1:n.4079G>C
(AP3B2)
|
|
|
|
ENST00000680492.1:n.4413G>C
(AP3B2)
|
|
|
|
ENST00000680912.1:n.2350G>C
(AP3B2)
|
|
|
|
ENST00000680946.1:n.3984G>C
(AP3B2)
|
|
|
|
ENST00000681044.1:n.4490G>C
(AP3B2)
|
|
|
|
ENST00000681327.1:c.*2779G>C
(AP3B2)
|
ENSP00000505423.1:n.*2779G>C
|
|
|
ENST00000681452.1:n.3339G>C
(AP3B2)
|
|
|
|
ENST00000681464.1:n.4286G>C
(AP3B2)
|
|
|
|
ENST00000261722.7:c.2933G>C
(AP3B2)
|
ENSP00000261722.3:p.Ser978Thr
|
|
|
ENST00000535348.5:c.2837G>C
(AP3B2)
|
ENSP00000438721.1:p.Ser946Thr
|
|
|
ENST00000535359.5:c.2990G>C
(AP3B2)
|
ENSP00000440984.1:p.Ser997Thr
|
|
|
ENST00000537735.1:n.601G>C
(AP3B2)
|
|
|
|
ENST00000543938.5:n.2056G>C
(AP3B2)
|
|
|
|
ENST00000620652.4:c.2933G>C
(AP3B2)
|
ENSP00000479229.1:p.Ser978Thr
|
|
|
NM_001278511.1:c.2837G>C
(AP3B2)
|
NP_001265440.1:p.Ser946Thr
|
|
|
NM_001278512.1:c.2990G>C
(AP3B2)
|
NP_001265441.1:p.Ser997Thr
|
|
|
NM_004644.4:c.2933G>C
(AP3B2)
|
NP_004635.2:p.Ser978Thr
|
|
|
NR_046096.1:n.1328+11705C>G
(CPEB1-AS1)
|
|
|
|
XM_011522097.1:c.2918G>C
(AP3B2)
|
XP_011520399.1:p.Ser973Thr
|
|
|
XM_011522098.1:c.2894G>C
(AP3B2)
|
XP_011520400.1:p.Ser965Thr
|
|
|
XM_011522100.1:c.1841G>C
(AP3B2)
|
XP_011520402.1:p.Ser614Thr
|
|
|
NM_001348441.1:c.122G>C
(AP3B2)
|
NP_001335370.1:p.Ser41Thr
|
|
|
XM_017022640.2:c.2861G>C
(AP3B2)
|
XP_016878129.1:p.Ser954Thr
|
|
|
XM_024450081.1:c.272G>C
(AP3B2)
|
XP_024305849.1:p.Ser91Thr
|
|
|
XM_024450082.1:c.122G>C
(AP3B2)
|
XP_024305850.1:p.Ser41Thr
|
|
|
XR_001751404.2:n.3161G>C
(AP3B2)
|
|
|
|
NM_001278512.2:c.2990G>C
(AP3B2)
MANE Select
|
NP_001265441.1:p.Ser997Thr
|
|
|
NM_004644.5:c.2933G>C
(AP3B2)
|
NP_004635.2:p.Ser978Thr
|
|
|
NM_001278511.2:c.2837G>C
(AP3B2)
|
NP_001265440.1:p.Ser946Thr
|
|
|
NM_001348441.2:c.122G>C
(AP3B2)
|
NP_001335370.1:p.Ser41Thr
|
|
