|
ENST00000261722.8:c.2891G>A
(AP3B2)
|
ENSP00000261722.4:p.Arg964Gln
|
|
|
ENST00000535359.6:c.2930G>A
(AP3B2)
MANE Select
|
ENSP00000440984.1:p.Arg977Gln
|
|
|
ENST00000535385.6:n.3817G>A
(AP3B2)
|
|
|
|
ENST00000537735.2:n.3019G>A
(AP3B2)
|
|
|
|
ENST00000543938.6:n.3517G>A
(AP3B2)
|
|
|
|
ENST00000642989.2:c.3002G>A
(AP3B2)
|
ENSP00000493485.1:p.Arg1001Gln
|
|
|
ENST00000652847.1:c.2873G>A
(AP3B2)
|
ENSP00000499785.1:p.Arg958Gln
|
|
|
ENST00000657321.1:c.*2719G>A
(AP3B2)
|
ENSP00000499716.1:n.*2719G>A
|
|
|
ENST00000660624.1:c.1781G>A
(AP3B2)
|
ENSP00000499379.1:p.Arg594Gln
|
|
|
ENST00000661532.1:c.2162G>A
(AP3B2)
|
|
|
|
ENST00000663651.1:n.3015G>A
(AP3B2)
|
|
|
|
ENST00000666973.1:c.2873G>A
(AP3B2)
|
ENSP00000499288.1:p.Arg958Gln
|
|
|
ENST00000667758.1:c.*3528G>A
(AP3B2)
|
ENSP00000499318.1:n.*3528G>A
|
|
|
ENST00000668385.1:c.*2671G>A
(AP3B2)
|
ENSP00000499544.1:n.*2671G>A
|
|
|
ENST00000668458.1:c.2621G>A
(AP3B2)
|
|
|
|
ENST00000668990.2:c.2873G>A
(AP3B2)
|
ENSP00000499235.1:p.Arg958Gln
|
|
|
ENST00000669930.1:c.2702G>A
(AP3B2)
|
ENSP00000499671.1:p.Arg901Gln
|
|
|
ENST00000679388.1:n.3457G>A
(AP3B2)
|
|
|
|
ENST00000679531.1:n.3720G>A
(AP3B2)
|
|
|
|
ENST00000679891.1:n.1751G>A
(AP3B2)
|
|
|
|
ENST00000679950.1:n.4019G>A
(AP3B2)
|
|
|
|
ENST00000680492.1:n.4353G>A
(AP3B2)
|
|
|
|
ENST00000680912.1:n.2290G>A
(AP3B2)
|
|
|
|
ENST00000680946.1:n.3924G>A
(AP3B2)
|
|
|
|
ENST00000681044.1:n.4430G>A
(AP3B2)
|
|
|
|
ENST00000681327.1:c.*2719G>A
(AP3B2)
|
ENSP00000505423.1:n.*2719G>A
|
|
|
ENST00000681452.1:n.3279G>A
(AP3B2)
|
|
|
|
ENST00000681464.1:n.4226G>A
(AP3B2)
|
|
|
|
ENST00000261722.7:c.2873G>A
(AP3B2)
|
ENSP00000261722.3:p.Arg958Gln
|
|
|
ENST00000535348.5:c.2777G>A
(AP3B2)
|
ENSP00000438721.1:p.Arg926Gln
|
|
|
ENST00000535359.5:c.2930G>A
(AP3B2)
|
ENSP00000440984.1:p.Arg977Gln
|
|
|
ENST00000537735.1:n.541G>A
(AP3B2)
|
|
|
|
ENST00000543938.5:n.1996G>A
(AP3B2)
|
|
|
|
ENST00000620652.4:c.2873G>A
(AP3B2)
|
ENSP00000479229.1:p.Arg958Gln
|
|
|
NM_001278511.1:c.2777G>A
(AP3B2)
|
NP_001265440.1:p.Arg926Gln
|
|
|
NM_001278512.1:c.2930G>A
(AP3B2)
|
NP_001265441.1:p.Arg977Gln
|
|
|
NM_004644.4:c.2873G>A
(AP3B2)
|
NP_004635.2:p.Arg958Gln
|
|
|
NR_046096.1:n.1328+11765C>T
(CPEB1-AS1)
|
|
|
|
XM_011522097.1:c.2858G>A
(AP3B2)
|
XP_011520399.1:p.Arg953Gln
|
|
|
XM_011522098.1:c.2834G>A
(AP3B2)
|
XP_011520400.1:p.Arg945Gln
|
|
|
XM_011522100.1:c.1781G>A
(AP3B2)
|
XP_011520402.1:p.Arg594Gln
|
|
|
NM_001348441.1:c.62G>A
(AP3B2)
|
NP_001335370.1:p.Arg21Gln
|
|
|
XM_017022640.2:c.2801G>A
(AP3B2)
|
XP_016878129.1:p.Arg934Gln
|
|
|
XM_024450081.1:c.212G>A
(AP3B2)
|
XP_024305849.1:p.Arg71Gln
|
|
|
XM_024450082.1:c.62G>A
(AP3B2)
|
XP_024305850.1:p.Arg21Gln
|
|
|
XR_001751404.2:n.3101G>A
(AP3B2)
|
|
|
|
NM_001278512.2:c.2930G>A
(AP3B2)
MANE Select
|
NP_001265441.1:p.Arg977Gln
|
|
|
NM_004644.5:c.2873G>A
(AP3B2)
|
NP_004635.2:p.Arg958Gln
|
|
|
NM_001278511.2:c.2777G>A
(AP3B2)
|
NP_001265440.1:p.Arg926Gln
|
|
|
NM_001348441.2:c.62G>A
(AP3B2)
|
NP_001335370.1:p.Arg21Gln
|
|
