|
ENST00000261722.8:c.2947A>G
(AP3B2)
|
ENSP00000261722.4:p.Met983Val
|
|
|
ENST00000535359.6:c.2986A>G
(AP3B2)
MANE Select
|
ENSP00000440984.1:p.Met996Val
|
|
|
ENST00000535385.6:n.3873A>G
(AP3B2)
|
|
|
|
ENST00000537735.2:n.3075A>G
(AP3B2)
|
|
|
|
ENST00000543938.6:n.3573A>G
(AP3B2)
|
|
|
|
ENST00000642989.2:c.3058A>G
(AP3B2)
|
ENSP00000493485.1:p.Met1020Val
|
|
|
ENST00000652847.1:c.2929A>G
(AP3B2)
|
ENSP00000499785.1:p.Met977Val
|
|
|
ENST00000657321.1:c.*2775A>G
(AP3B2)
|
ENSP00000499716.1:n.*2775A>G
|
|
|
ENST00000660624.1:c.1837A>G
(AP3B2)
|
ENSP00000499379.1:p.Met613Val
|
|
|
ENST00000661532.1:c.2218A>G
(AP3B2)
|
|
|
|
ENST00000663651.1:n.3071A>G
(AP3B2)
|
|
|
|
ENST00000666973.1:c.2929A>G
(AP3B2)
|
ENSP00000499288.1:p.Met977Val
|
|
|
ENST00000667758.1:c.*3584A>G
(AP3B2)
|
ENSP00000499318.1:n.*3584A>G
|
|
|
ENST00000668385.1:c.*2727A>G
(AP3B2)
|
ENSP00000499544.1:n.*2727A>G
|
|
|
ENST00000668458.1:c.2677A>G
(AP3B2)
|
|
|
|
ENST00000668990.2:c.2929A>G
(AP3B2)
|
ENSP00000499235.1:p.Met977Val
|
|
|
ENST00000669930.1:c.2758A>G
(AP3B2)
|
ENSP00000499671.1:p.Met920Val
|
|
|
ENST00000679388.1:n.3513A>G
(AP3B2)
|
|
|
|
ENST00000679531.1:n.3776A>G
(AP3B2)
|
|
|
|
ENST00000679891.1:n.1807A>G
(AP3B2)
|
|
|
|
ENST00000679950.1:n.4075A>G
(AP3B2)
|
|
|
|
ENST00000680492.1:n.4409A>G
(AP3B2)
|
|
|
|
ENST00000680912.1:n.2346A>G
(AP3B2)
|
|
|
|
ENST00000680946.1:n.3980A>G
(AP3B2)
|
|
|
|
ENST00000681044.1:n.4486A>G
(AP3B2)
|
|
|
|
ENST00000681327.1:c.*2775A>G
(AP3B2)
|
ENSP00000505423.1:n.*2775A>G
|
|
|
ENST00000681452.1:n.3335A>G
(AP3B2)
|
|
|
|
ENST00000681464.1:n.4282A>G
(AP3B2)
|
|
|
|
ENST00000261722.7:c.2929A>G
(AP3B2)
|
ENSP00000261722.3:p.Met977Val
|
|
|
ENST00000535348.5:c.2833A>G
(AP3B2)
|
ENSP00000438721.1:p.Met945Val
|
|
|
ENST00000535359.5:c.2986A>G
(AP3B2)
|
ENSP00000440984.1:p.Met996Val
|
|
|
ENST00000537735.1:n.597A>G
(AP3B2)
|
|
|
|
ENST00000543938.5:n.2052A>G
(AP3B2)
|
|
|
|
ENST00000620652.4:c.2929A>G
(AP3B2)
|
ENSP00000479229.1:p.Met977Val
|
|
|
NM_001278511.1:c.2833A>G
(AP3B2)
|
NP_001265440.1:p.Met945Val
|
|
|
NM_001278512.1:c.2986A>G
(AP3B2)
|
NP_001265441.1:p.Met996Val
|
|
|
NM_004644.4:c.2929A>G
(AP3B2)
|
NP_004635.2:p.Met977Val
|
|
|
NR_046096.1:n.1328+11709T>C
(CPEB1-AS1)
|
|
|
|
XM_011522097.1:c.2914A>G
(AP3B2)
|
XP_011520399.1:p.Met972Val
|
|
|
XM_011522098.1:c.2890A>G
(AP3B2)
|
XP_011520400.1:p.Met964Val
|
|
|
XM_011522100.1:c.1837A>G
(AP3B2)
|
XP_011520402.1:p.Met613Val
|
|
|
NM_001348441.1:c.118A>G
(AP3B2)
|
NP_001335370.1:p.Met40Val
|
|
|
XM_017022640.2:c.2857A>G
(AP3B2)
|
XP_016878129.1:p.Met953Val
|
|
|
XM_024450081.1:c.268A>G
(AP3B2)
|
XP_024305849.1:p.Met90Val
|
|
|
XM_024450082.1:c.118A>G
(AP3B2)
|
XP_024305850.1:p.Met40Val
|
|
|
XR_001751404.2:n.3157A>G
(AP3B2)
|
|
|
|
NM_001278512.2:c.2986A>G
(AP3B2)
MANE Select
|
NP_001265441.1:p.Met996Val
|
|
|
NM_004644.5:c.2929A>G
(AP3B2)
|
NP_004635.2:p.Met977Val
|
|
|
NM_001278511.2:c.2833A>G
(AP3B2)
|
NP_001265440.1:p.Met945Val
|
|
|
NM_001348441.2:c.118A>G
(AP3B2)
|
NP_001335370.1:p.Met40Val
|
|
