|
ENST00000261722.8:c.3208G>A
(AP3B2)
|
ENSP00000261722.4:p.Glu1070Lys
|
|
|
ENST00000535359.6:c.3247G>A
(AP3B2)
MANE Select
|
ENSP00000440984.1:p.Glu1083Lys
|
|
|
ENST00000535385.6:n.4134G>A
(AP3B2)
|
|
|
|
ENST00000537735.2:n.3336G>A
(AP3B2)
|
|
|
|
ENST00000543938.6:n.3834G>A
(AP3B2)
|
|
|
|
ENST00000642989.2:c.3319G>A
(AP3B2)
|
ENSP00000493485.1:p.Glu1107Lys
|
|
|
ENST00000652847.1:c.3221G>A
(AP3B2)
|
ENSP00000499785.1:p.Arg1074Gln
|
|
|
ENST00000657321.1:c.*3036G>A
(AP3B2)
|
ENSP00000499716.1:n.*3036G>A
|
|
|
ENST00000660624.1:c.2098G>A
(AP3B2)
|
ENSP00000499379.1:p.Glu700Lys
|
|
|
ENST00000661532.1:c.2479G>A
(AP3B2)
|
|
|
|
ENST00000663651.1:n.3332G>A
(AP3B2)
|
|
|
|
ENST00000666973.1:c.*72G>A
(AP3B2)
|
ENSP00000499288.1:n.*72G>A
|
|
|
ENST00000667758.1:c.*3845G>A
(AP3B2)
|
ENSP00000499318.1:n.*3845G>A
|
|
|
ENST00000668385.1:c.*2988G>A
(AP3B2)
|
ENSP00000499544.1:n.*2988G>A
|
|
|
ENST00000668990.2:c.3190G>A
(AP3B2)
|
ENSP00000499235.1:p.Glu1064Lys
|
|
|
ENST00000669930.1:c.3019G>A
(AP3B2)
|
ENSP00000499671.1:p.Glu1007Lys
|
|
|
ENST00000679388.1:n.3774G>A
(AP3B2)
|
|
|
|
ENST00000679531.1:n.5878G>A
(AP3B2)
|
|
|
|
ENST00000679891.1:n.2068G>A
(AP3B2)
|
|
|
|
ENST00000679950.1:n.4336G>A
(AP3B2)
|
|
|
|
ENST00000680492.1:n.4670G>A
(AP3B2)
|
|
|
|
ENST00000680912.1:n.2607G>A
(AP3B2)
|
|
|
|
ENST00000680946.1:n.4241G>A
(AP3B2)
|
|
|
|
ENST00000681044.1:n.4747G>A
(AP3B2)
|
|
|
|
ENST00000681327.1:c.*3036G>A
(AP3B2)
|
ENSP00000505423.1:n.*3036G>A
|
|
|
ENST00000681452.1:n.5437G>A
(AP3B2)
|
|
|
|
ENST00000681464.1:n.4543G>A
(AP3B2)
|
|
|
|
ENST00000261722.7:c.3190G>A
(AP3B2)
|
ENSP00000261722.3:p.Glu1064Lys
|
|
|
ENST00000535348.5:c.3094G>A
(AP3B2)
|
ENSP00000438721.1:p.Glu1032Lys
|
|
|
ENST00000535359.5:c.3247G>A
(AP3B2)
|
ENSP00000440984.1:p.Glu1083Lys
|
|
|
ENST00000537735.1:n.858G>A
(AP3B2)
|
|
|
|
ENST00000543938.5:n.2313G>A
(AP3B2)
|
|
|
|
ENST00000620652.4:c.3190G>A
(AP3B2)
|
ENSP00000479229.1:p.Glu1064Lys
|
|
|
NM_001278511.1:c.3094G>A
(AP3B2)
|
NP_001265440.1:p.Glu1032Lys
|
|
|
NM_001278512.1:c.3247G>A
(AP3B2)
|
NP_001265441.1:p.Glu1083Lys
|
|
|
NM_004644.4:c.3190G>A
(AP3B2)
|
NP_004635.2:p.Glu1064Lys
|
|
|
NR_046096.1:n.1328+9473C>T
(CPEB1-AS1)
|
|
|
|
XM_011522097.1:c.3175G>A
(AP3B2)
|
XP_011520399.1:p.Glu1059Lys
|
|
|
XM_011522098.1:c.3151G>A
(AP3B2)
|
XP_011520400.1:p.Glu1051Lys
|
|
|
XM_011522100.1:c.2098G>A
(AP3B2)
|
XP_011520402.1:p.Glu700Lys
|
|
|
NM_001348441.1:c.379G>A
(AP3B2)
|
NP_001335370.1:p.Glu127Lys
|
|
|
XM_017022640.2:c.3118G>A
(AP3B2)
|
XP_016878129.1:p.Glu1040Lys
|
|
|
XM_024450081.1:c.529G>A
(AP3B2)
|
XP_024305849.1:p.Glu177Lys
|
|
|
XM_024450082.1:c.379G>A
(AP3B2)
|
XP_024305850.1:p.Glu127Lys
|
|
|
XR_001751404.2:n.3418G>A
(AP3B2)
|
|
|
|
NM_001278512.2:c.3247G>A
(AP3B2)
MANE Select
|
NP_001265441.1:p.Glu1083Lys
|
|
|
NM_004644.5:c.3190G>A
(AP3B2)
|
NP_004635.2:p.Glu1064Lys
|
|
|
NM_001278511.2:c.3094G>A
(AP3B2)
|
NP_001265440.1:p.Glu1032Lys
|
|
|
NM_001348441.2:c.379G>A
(AP3B2)
|
NP_001335370.1:p.Glu127Lys
|
|
