|
ENST00000261722.8:c.3085C>A
(AP3B2)
|
ENSP00000261722.4:p.Arg1029Ser
|
|
|
ENST00000535359.6:c.3124C>A
(AP3B2)
MANE Select
|
ENSP00000440984.1:p.Arg1042Ser
|
|
|
ENST00000535385.6:n.4011C>A
(AP3B2)
|
|
|
|
ENST00000537735.2:n.3213C>A
(AP3B2)
|
|
|
|
ENST00000543938.6:n.3711C>A
(AP3B2)
|
|
|
|
ENST00000642989.2:c.3196C>A
(AP3B2)
|
ENSP00000493485.1:p.Arg1066Ser
|
|
|
ENST00000652847.1:c.3067C>A
(AP3B2)
|
ENSP00000499785.1:p.Arg1023Ser
|
|
|
ENST00000657321.1:c.*2913C>A
(AP3B2)
|
ENSP00000499716.1:n.*2913C>A
|
|
|
ENST00000660624.1:c.1975C>A
(AP3B2)
|
ENSP00000499379.1:p.Arg659Ser
|
|
|
ENST00000661532.1:c.2356C>A
(AP3B2)
|
|
|
|
ENST00000663651.1:n.3209C>A
(AP3B2)
|
|
|
|
ENST00000666973.1:c.2960-166C>A
(AP3B2)
|
ENSP00000499288.1:n.2960-166C>A
|
|
|
ENST00000667758.1:c.*3722C>A
(AP3B2)
|
ENSP00000499318.1:n.*3722C>A
|
|
|
ENST00000668385.1:c.*2865C>A
(AP3B2)
|
ENSP00000499544.1:n.*2865C>A
|
|
|
ENST00000668990.2:c.3067C>A
(AP3B2)
|
ENSP00000499235.1:p.Arg1023Ser
|
|
|
ENST00000669930.1:c.2896C>A
(AP3B2)
|
ENSP00000499671.1:p.Arg966Ser
|
|
|
ENST00000679388.1:n.3651C>A
(AP3B2)
|
|
|
|
ENST00000679531.1:n.5755C>A
(AP3B2)
|
|
|
|
ENST00000679891.1:n.1945C>A
(AP3B2)
|
|
|
|
ENST00000679950.1:n.4213C>A
(AP3B2)
|
|
|
|
ENST00000680492.1:n.4547C>A
(AP3B2)
|
|
|
|
ENST00000680912.1:n.2484C>A
(AP3B2)
|
|
|
|
ENST00000680946.1:n.4118C>A
(AP3B2)
|
|
|
|
ENST00000681044.1:n.4624C>A
(AP3B2)
|
|
|
|
ENST00000681327.1:c.*2913C>A
(AP3B2)
|
ENSP00000505423.1:n.*2913C>A
|
|
|
ENST00000681452.1:n.5314C>A
(AP3B2)
|
|
|
|
ENST00000681464.1:n.4420C>A
(AP3B2)
|
|
|
|
ENST00000261722.7:c.3067C>A
(AP3B2)
|
ENSP00000261722.3:p.Arg1023Ser
|
|
|
ENST00000535348.5:c.2971C>A
(AP3B2)
|
ENSP00000438721.1:p.Arg991Ser
|
|
|
ENST00000535359.5:c.3124C>A
(AP3B2)
|
ENSP00000440984.1:p.Arg1042Ser
|
|
|
ENST00000537735.1:n.735C>A
(AP3B2)
|
|
|
|
ENST00000543938.5:n.2190C>A
(AP3B2)
|
|
|
|
ENST00000620652.4:c.3067C>A
(AP3B2)
|
ENSP00000479229.1:p.Arg1023Ser
|
|
|
NM_001278511.1:c.2971C>A
(AP3B2)
|
NP_001265440.1:p.Arg991Ser
|
|
|
NM_001278512.1:c.3124C>A
(AP3B2)
|
NP_001265441.1:p.Arg1042Ser
|
|
|
NM_004644.4:c.3067C>A
(AP3B2)
|
NP_004635.2:p.Arg1023Ser
|
|
|
NR_046096.1:n.1328+9730G>T
(CPEB1-AS1)
|
|
|
|
XM_011522097.1:c.3052C>A
(AP3B2)
|
XP_011520399.1:p.Arg1018Ser
|
|
|
XM_011522098.1:c.3028C>A
(AP3B2)
|
XP_011520400.1:p.Arg1010Ser
|
|
|
XM_011522100.1:c.1975C>A
(AP3B2)
|
XP_011520402.1:p.Arg659Ser
|
|
|
NM_001348441.1:c.256C>A
(AP3B2)
|
NP_001335370.1:p.Arg86Ser
|
|
|
XM_017022640.2:c.2995C>A
(AP3B2)
|
XP_016878129.1:p.Arg999Ser
|
|
|
XM_024450081.1:c.406C>A
(AP3B2)
|
XP_024305849.1:p.Arg136Ser
|
|
|
XM_024450082.1:c.256C>A
(AP3B2)
|
XP_024305850.1:p.Arg86Ser
|
|
|
XR_001751404.2:n.3295C>A
(AP3B2)
|
|
|
|
NM_001278512.2:c.3124C>A
(AP3B2)
MANE Select
|
NP_001265441.1:p.Arg1042Ser
|
|
|
NM_004644.5:c.3067C>A
(AP3B2)
|
NP_004635.2:p.Arg1023Ser
|
|
|
NM_001278511.2:c.2971C>A
(AP3B2)
|
NP_001265440.1:p.Arg991Ser
|
|
|
NM_001348441.2:c.256C>A
(AP3B2)
|
NP_001335370.1:p.Arg86Ser
|
|
