|
ENST00000261722.8:c.2949G>A
(AP3B2)
|
ENSP00000261722.4:p.Met983Ile
|
|
|
ENST00000535359.6:c.2988G>A
(AP3B2)
MANE Select
|
ENSP00000440984.1:p.Met996Ile
|
|
|
ENST00000535385.6:n.3875G>A
(AP3B2)
|
|
|
|
ENST00000537735.2:n.3077G>A
(AP3B2)
|
|
|
|
ENST00000543938.6:n.3575G>A
(AP3B2)
|
|
|
|
ENST00000642989.2:c.3060G>A
(AP3B2)
|
ENSP00000493485.1:p.Met1020Ile
|
|
|
ENST00000652847.1:c.2931G>A
(AP3B2)
|
ENSP00000499785.1:p.Met977Ile
|
|
|
ENST00000657321.1:c.*2777G>A
(AP3B2)
|
ENSP00000499716.1:n.*2777G>A
|
|
|
ENST00000660624.1:c.1839G>A
(AP3B2)
|
ENSP00000499379.1:p.Met613Ile
|
|
|
ENST00000661532.1:c.2220G>A
(AP3B2)
|
|
|
|
ENST00000663651.1:n.3073G>A
(AP3B2)
|
|
|
|
ENST00000666973.1:c.2931G>A
(AP3B2)
|
ENSP00000499288.1:p.Met977Ile
|
|
|
ENST00000667758.1:c.*3586G>A
(AP3B2)
|
ENSP00000499318.1:n.*3586G>A
|
|
|
ENST00000668385.1:c.*2729G>A
(AP3B2)
|
ENSP00000499544.1:n.*2729G>A
|
|
|
ENST00000668458.1:c.2679G>A
(AP3B2)
|
|
|
|
ENST00000668990.2:c.2931G>A
(AP3B2)
|
ENSP00000499235.1:p.Met977Ile
|
|
|
ENST00000669930.1:c.2760G>A
(AP3B2)
|
ENSP00000499671.1:p.Met920Ile
|
|
|
ENST00000679388.1:n.3515G>A
(AP3B2)
|
|
|
|
ENST00000679531.1:n.3778G>A
(AP3B2)
|
|
|
|
ENST00000679891.1:n.1809G>A
(AP3B2)
|
|
|
|
ENST00000679950.1:n.4077G>A
(AP3B2)
|
|
|
|
ENST00000680492.1:n.4411G>A
(AP3B2)
|
|
|
|
ENST00000680912.1:n.2348G>A
(AP3B2)
|
|
|
|
ENST00000680946.1:n.3982G>A
(AP3B2)
|
|
|
|
ENST00000681044.1:n.4488G>A
(AP3B2)
|
|
|
|
ENST00000681327.1:c.*2777G>A
(AP3B2)
|
ENSP00000505423.1:n.*2777G>A
|
|
|
ENST00000681452.1:n.3337G>A
(AP3B2)
|
|
|
|
ENST00000681464.1:n.4284G>A
(AP3B2)
|
|
|
|
ENST00000261722.7:c.2931G>A
(AP3B2)
|
ENSP00000261722.3:p.Met977Ile
|
|
|
ENST00000535348.5:c.2835G>A
(AP3B2)
|
ENSP00000438721.1:p.Met945Ile
|
|
|
ENST00000535359.5:c.2988G>A
(AP3B2)
|
ENSP00000440984.1:p.Met996Ile
|
|
|
ENST00000537735.1:n.599G>A
(AP3B2)
|
|
|
|
ENST00000543938.5:n.2054G>A
(AP3B2)
|
|
|
|
ENST00000620652.4:c.2931G>A
(AP3B2)
|
ENSP00000479229.1:p.Met977Ile
|
|
|
NM_001278511.1:c.2835G>A
(AP3B2)
|
NP_001265440.1:p.Met945Ile
|
|
|
NM_001278512.1:c.2988G>A
(AP3B2)
|
NP_001265441.1:p.Met996Ile
|
|
|
NM_004644.4:c.2931G>A
(AP3B2)
|
NP_004635.2:p.Met977Ile
|
|
|
NR_046096.1:n.1328+11707C>T
(CPEB1-AS1)
|
|
|
|
XM_011522097.1:c.2916G>A
(AP3B2)
|
XP_011520399.1:p.Met972Ile
|
|
|
XM_011522098.1:c.2892G>A
(AP3B2)
|
XP_011520400.1:p.Met964Ile
|
|
|
XM_011522100.1:c.1839G>A
(AP3B2)
|
XP_011520402.1:p.Met613Ile
|
|
|
NM_001348441.1:c.120G>A
(AP3B2)
|
NP_001335370.1:p.Met40Ile
|
|
|
XM_017022640.2:c.2859G>A
(AP3B2)
|
XP_016878129.1:p.Met953Ile
|
|
|
XM_024450081.1:c.270G>A
(AP3B2)
|
XP_024305849.1:p.Met90Ile
|
|
|
XM_024450082.1:c.120G>A
(AP3B2)
|
XP_024305850.1:p.Met40Ile
|
|
|
XR_001751404.2:n.3159G>A
(AP3B2)
|
|
|
|
NM_001278512.2:c.2988G>A
(AP3B2)
MANE Select
|
NP_001265441.1:p.Met996Ile
|
|
|
NM_004644.5:c.2931G>A
(AP3B2)
|
NP_004635.2:p.Met977Ile
|
|
|
NM_001278511.2:c.2835G>A
(AP3B2)
|
NP_001265440.1:p.Met945Ile
|
|
|
NM_001348441.2:c.120G>A
(AP3B2)
|
NP_001335370.1:p.Met40Ile
|
|
