ENST00000261722.8:c.2977+15G>A
(AP3B2)
|
ENSP00000261722.4:n.2977+15G>A
|
|
ENST00000535359.6:c.3016+15G>A
(AP3B2)
MANE Select
|
ENSP00000440984.1:n.3016+15G>A
|
|
ENST00000535385.6:n.3903+15G>A
(AP3B2)
|
|
|
ENST00000537735.2:n.3105+15G>A
(AP3B2)
|
|
|
ENST00000543938.6:n.3603+15G>A
(AP3B2)
|
|
|
ENST00000642989.2:c.3088+15G>A
(AP3B2)
|
ENSP00000493485.1:n.3088+15G>A
|
|
ENST00000652847.1:c.2959+15G>A
(AP3B2)
|
ENSP00000499785.1:n.2959+15G>A
|
|
ENST00000657321.1:c.*2805+15G>A
(AP3B2)
|
ENSP00000499716.1:n.*2805+15G>A
|
|
ENST00000660624.1:c.1867+15G>A
(AP3B2)
|
ENSP00000499379.1:n.1867+15G>A
|
|
ENST00000661532.1:c.2248+15G>A
(AP3B2)
|
|
|
ENST00000663651.1:n.3101+15G>A
(AP3B2)
|
|
|
ENST00000666973.1:c.2959+15G>A
(AP3B2)
|
ENSP00000499288.1:n.2959+15G>A
|
|
ENST00000667758.1:c.*3614+15G>A
(AP3B2)
|
ENSP00000499318.1:n.*3614+15G>A
|
|
ENST00000668385.1:c.*2757+15G>A
(AP3B2)
|
ENSP00000499544.1:n.*2757+15G>A
|
|
ENST00000668458.1:c.2707+15G>A
(AP3B2)
|
|
|
ENST00000668990.2:c.2959+15G>A
(AP3B2)
|
ENSP00000499235.1:n.2959+15G>A
|
|
ENST00000669930.1:c.2788+15G>A
(AP3B2)
|
ENSP00000499671.1:n.2788+15G>A
|
|
ENST00000679388.1:n.3543+15G>A
(AP3B2)
|
|
|
ENST00000679531.1:n.3821G>A
(AP3B2)
|
|
|
ENST00000679891.1:n.1837+15G>A
(AP3B2)
|
|
|
ENST00000679950.1:n.4105+15G>A
(AP3B2)
|
|
|
ENST00000680492.1:n.4439+15G>A
(AP3B2)
|
|
|
ENST00000680912.1:n.2376+15G>A
(AP3B2)
|
|
|
ENST00000680946.1:n.4010+15G>A
(AP3B2)
|
|
|
ENST00000681044.1:n.4516+15G>A
(AP3B2)
|
|
|
ENST00000681327.1:c.*2805+15G>A
(AP3B2)
|
ENSP00000505423.1:n.*2805+15G>A
|
|
ENST00000681452.1:n.3380G>A
(AP3B2)
|
|
|
ENST00000681464.1:n.4312+15G>A
(AP3B2)
|
|
|
ENST00000261722.7:c.2959+15G>A
(AP3B2)
|
ENSP00000261722.3:n.2959+15G>A
|
|
ENST00000535348.5:c.2863+15G>A
(AP3B2)
|
ENSP00000438721.1:n.2863+15G>A
|
|
ENST00000535359.5:c.3016+15G>A
(AP3B2)
|
ENSP00000440984.1:n.3016+15G>A
|
|
ENST00000537735.1:n.627+15G>A
(AP3B2)
|
|
|
ENST00000543938.5:n.2082+15G>A
(AP3B2)
|
|
|
ENST00000620652.4:c.2959+15G>A
(AP3B2)
|
ENSP00000479229.1:n.2959+15G>A
|
|
NM_001278511.1:c.2863+15G>A
(AP3B2)
|
NP_001265440.1:n.2863+15G>A
|
|
NM_001278512.1:c.3016+15G>A
(AP3B2)
|
NP_001265441.1:n.3016+15G>A
|
|
NM_004644.4:c.2959+15G>A
(AP3B2)
|
NP_004635.2:n.2959+15G>A
|
|
NR_046096.1:n.1328+11664C>T
(CPEB1-AS1)
|
|
|
XM_011522097.1:c.2944+15G>A
(AP3B2)
|
XP_011520399.1:n.2944+15G>A
|
|
XM_011522098.1:c.2920+15G>A
(AP3B2)
|
XP_011520400.1:n.2920+15G>A
|
|
XM_011522100.1:c.1867+15G>A
(AP3B2)
|
XP_011520402.1:n.1867+15G>A
|
|
NM_001348441.1:c.148+15G>A
(AP3B2)
|
NP_001335370.1:n.148+15G>A
|
|
XM_017022640.2:c.2887+15G>A
(AP3B2)
|
XP_016878129.1:n.2887+15G>A
|
|
XM_024450081.1:c.298+15G>A
(AP3B2)
|
XP_024305849.1:n.298+15G>A
|
|
XM_024450082.1:c.148+15G>A
(AP3B2)
|
XP_024305850.1:n.148+15G>A
|
|
XR_001751404.2:n.3187+15G>A
(AP3B2)
|
|
|
NM_001278512.2:c.3016+15G>A
(AP3B2)
MANE Select
|
NP_001265441.1:n.3016+15G>A
|
|
NM_004644.5:c.2959+15G>A
(AP3B2)
|
NP_004635.2:n.2959+15G>A
|
|
NM_001278511.2:c.2863+15G>A
(AP3B2)
|
NP_001265440.1:n.2863+15G>A
|
|
NM_001348441.2:c.148+15G>A
(AP3B2)
|
NP_001335370.1:n.148+15G>A
|
|