|
ENST00000261722.8:c.1110+1G>C
(AP3B2)
|
ENSP00000261722.4:n.1110+1G>C
|
|
|
ENST00000535359.6:c.1110+1G>C
(AP3B2)
MANE Select
|
ENSP00000440984.1:n.1110+1G>C
|
|
|
ENST00000535385.6:n.1613+1G>C
(AP3B2)
|
|
|
|
ENST00000537735.2:n.1256+1G>C
(AP3B2)
|
|
|
|
ENST00000543938.6:n.1313+1G>C
(AP3B2)
|
|
|
|
ENST00000642989.2:c.1239+1G>C
(AP3B2)
|
ENSP00000493485.1:n.1239+1G>C
|
|
|
ENST00000652847.1:c.1110+1G>C
(AP3B2)
|
ENSP00000499785.1:n.1110+1G>C
|
|
|
ENST00000657321.1:c.*734+1G>C
(AP3B2)
|
ENSP00000499716.1:n.*734+1G>C
|
|
|
ENST00000660624.1:c.18+1G>C
(AP3B2)
|
ENSP00000499379.1:n.18+1G>C
|
|
|
ENST00000661532.1:c.337+1G>C
(AP3B2)
|
|
|
|
ENST00000663651.1:n.1252+1G>C
(AP3B2)
|
|
|
|
ENST00000664460.1:c.1014+1G>C
(AP3B2)
|
ENSP00000499798.1:n.1014+1G>C
|
|
|
ENST00000666055.1:c.1110+1G>C
(AP3B2)
|
ENSP00000499608.1:n.1110+1G>C
|
|
|
ENST00000666894.1:c.18+1G>C
(AP3B2)
|
ENSP00000499678.1:n.18+1G>C
|
|
|
ENST00000666973.1:c.1110+1G>C
(AP3B2)
|
ENSP00000499288.1:n.1110+1G>C
|
|
|
ENST00000667758.1:c.*998+1G>C
(AP3B2)
|
ENSP00000499318.1:n.*998+1G>C
|
|
|
ENST00000668385.1:c.*908+1G>C
(AP3B2)
|
ENSP00000499544.1:n.*908+1G>C
|
|
|
ENST00000668458.1:c.731+1G>C
(AP3B2)
|
|
|
|
ENST00000668990.2:c.1110+1G>C
(AP3B2)
|
ENSP00000499235.1:n.1110+1G>C
|
|
|
ENST00000669880.1:n.224+1G>C
(AP3B2)
|
|
|
|
ENST00000669930.1:c.939+1G>C
(AP3B2)
|
ENSP00000499671.1:n.939+1G>C
|
|
|
ENST00000679388.1:n.1049+1G>C
(AP3B2)
|
|
|
|
ENST00000679531.1:n.1516+1G>C
(AP3B2)
|
|
|
|
ENST00000679950.1:n.1489+1G>C
(AP3B2)
|
|
|
|
ENST00000680492.1:n.1516+1G>C
(AP3B2)
|
|
|
|
ENST00000680946.1:n.1516+1G>C
(AP3B2)
|
|
|
|
ENST00000681044.1:n.1516+1G>C
(AP3B2)
|
|
|
|
ENST00000681327.1:c.*734+1G>C
(AP3B2)
|
ENSP00000505423.1:n.*734+1G>C
|
|
|
ENST00000681452.1:n.1516+1G>C
(AP3B2)
|
|
|
|
ENST00000681464.1:n.1516+1G>C
(AP3B2)
|
|
|
|
ENST00000261722.7:c.1110+1G>C
(AP3B2)
|
ENSP00000261722.3:n.1110+1G>C
|
|
|
ENST00000535348.5:c.1014+1G>C
(AP3B2)
|
ENSP00000438721.1:n.1014+1G>C
|
|
|
ENST00000535359.5:c.1110+1G>C
(AP3B2)
|
ENSP00000440984.1:n.1110+1G>C
|
|
|
ENST00000543938.5:n.233+1G>C
(AP3B2)
|
|
|
|
ENST00000620652.4:c.1110+1G>C
(AP3B2)
|
ENSP00000479229.1:n.1110+1G>C
|
|
|
NM_001278511.1:c.1014+1G>C
(AP3B2)
|
NP_001265440.1:n.1014+1G>C
|
|
|
NM_001278512.1:c.1110+1G>C
(AP3B2)
|
NP_001265441.1:n.1110+1G>C
|
|
|
NM_004644.4:c.1110+1G>C
(AP3B2)
|
NP_004635.2:n.1110+1G>C
|
|
|
NR_046096.1:n.1329-11837C>G
(CPEB1-AS1)
|
|
|
|
XM_011522097.1:c.1110+1G>C
(AP3B2)
|
XP_011520399.1:n.1110+1G>C
|
|
|
XM_011522098.1:c.1014+1G>C
(AP3B2)
|
XP_011520400.1:n.1014+1G>C
|
|
|
XM_011522099.1:c.1110+1G>C
(AP3B2)
|
XP_011520401.1:n.1110+1G>C
|
|
|
XM_011522100.1:c.18+1G>C
(AP3B2)
|
XP_011520402.1:n.18+1G>C
|
|
|
XM_017022640.2:c.1110+1G>C
(AP3B2)
|
XP_016878129.1:n.1110+1G>C
|
|
|
XM_017022641.2:c.1110+1G>C
(AP3B2)
|
XP_016878130.1:n.1110+1G>C
|
|
|
XR_001751404.2:n.1276+1G>C
(AP3B2)
|
|
|
|
NM_001278512.2:c.1110+1G>C
(AP3B2)
MANE Select
|
NP_001265441.1:n.1110+1G>C
|
|
|
NM_004644.5:c.1110+1G>C
(AP3B2)
|
NP_004635.2:n.1110+1G>C
|
|
|
NM_001278511.2:c.1014+1G>C
(AP3B2)
|
NP_001265440.1:n.1014+1G>C
|
|
