ENST00000261722.8:c.2533C>T
(AP3B2)
|
ENSP00000261722.4:p.Leu845=
|
|
ENST00000535359.6:c.2572C>T
(AP3B2)
MANE Select
|
ENSP00000440984.1:p.Leu858=
|
|
ENST00000535385.6:n.3018C>T
(AP3B2)
|
|
|
ENST00000537735.2:n.2661C>T
(AP3B2)
|
|
|
ENST00000543938.6:n.2718C>T
(AP3B2)
|
|
|
ENST00000642989.2:c.2644C>T
(AP3B2)
|
ENSP00000493485.1:p.Leu882=
|
|
ENST00000652847.1:c.2515C>T
(AP3B2)
|
ENSP00000499785.1:p.Leu839=
|
|
ENST00000657321.1:c.*2590C>T
(AP3B2)
|
ENSP00000499716.1:n.*2590C>T
|
|
ENST00000660624.1:c.1423C>T
(AP3B2)
|
ENSP00000499379.1:p.Leu475=
|
|
ENST00000661532.1:c.1804C>T
(AP3B2)
|
|
|
ENST00000663651.1:n.2657C>T
(AP3B2)
|
|
|
ENST00000666973.1:c.2515C>T
(AP3B2)
|
ENSP00000499288.1:p.Leu839=
|
|
ENST00000667758.1:c.*2729C>T
(AP3B2)
|
ENSP00000499318.1:n.*2729C>T
|
|
ENST00000668385.1:c.*2313C>T
(AP3B2)
|
ENSP00000499544.1:n.*2313C>T
|
|
ENST00000668458.1:c.2263C>T
(AP3B2)
|
|
|
ENST00000668990.2:c.2515C>T
(AP3B2)
|
ENSP00000499235.1:p.Leu839=
|
|
ENST00000669930.1:c.2344C>T
(AP3B2)
|
ENSP00000499671.1:p.Leu782=
|
|
ENST00000679388.1:n.2454C>T
(AP3B2)
|
|
|
ENST00000679531.1:n.2921C>T
(AP3B2)
|
|
|
ENST00000679891.1:n.952C>T
(AP3B2)
|
|
|
ENST00000679950.1:n.3220C>T
(AP3B2)
|
|
|
ENST00000680492.1:n.3554C>T
(AP3B2)
|
|
|
ENST00000680912.1:n.1491C>T
(AP3B2)
|
|
|
ENST00000680946.1:n.2921C>T
(AP3B2)
|
|
|
ENST00000681044.1:n.3427C>T
(AP3B2)
|
|
|
ENST00000681327.1:c.*2590C>T
(AP3B2)
|
ENSP00000505423.1:n.*2590C>T
|
|
ENST00000681452.1:n.2921C>T
(AP3B2)
|
|
|
ENST00000681464.1:n.3427C>T
(AP3B2)
|
|
|
ENST00000261722.7:c.2515C>T
(AP3B2)
|
ENSP00000261722.3:p.Leu839=
|
|
ENST00000535348.5:c.2419C>T
(AP3B2)
|
ENSP00000438721.1:p.Leu807=
|
|
ENST00000535359.5:c.2572C>T
(AP3B2)
|
ENSP00000440984.1:p.Leu858=
|
|
ENST00000538592.1:c.162C>T
(AP3B2)
|
ENSP00000445804.1:n.162C>T
|
|
ENST00000543938.5:n.1638C>T
(AP3B2)
|
|
|
ENST00000545315.1:n.91C>T
(AP3B2)
|
|
|
ENST00000620652.4:c.2515C>T
(AP3B2)
|
ENSP00000479229.1:p.Leu839=
|
|
NM_001278511.1:c.2419C>T
(AP3B2)
|
NP_001265440.1:p.Leu807=
|
|
NM_001278512.1:c.2572C>T
(AP3B2)
|
NP_001265441.1:p.Leu858=
|
|
NM_004644.4:c.2515C>T
(AP3B2)
|
NP_004635.2:p.Leu839=
|
|
NR_046096.1:n.1328+13013G>A
(CPEB1-AS1)
|
|
|
XM_011522097.1:c.2500C>T
(AP3B2)
|
XP_011520399.1:p.Leu834=
|
|
XM_011522098.1:c.2476C>T
(AP3B2)
|
XP_011520400.1:p.Leu826=
|
|
XM_011522100.1:c.1423C>T
(AP3B2)
|
XP_011520402.1:p.Leu475=
|
|
XM_017022640.2:c.2443C>T
(AP3B2)
|
XP_016878129.1:p.Leu815=
|
|
XM_024450081.1:c.-147C>T
(AP3B2)
|
XP_024305849.1:n.-147C>T
|
|
XM_024450082.1:c.-738C>T
(AP3B2)
|
XP_024305850.1:n.-738C>T
|
|
XR_001751404.2:n.2743C>T
(AP3B2)
|
|
|
NM_001278512.2:c.2572C>T
(AP3B2)
MANE Select
|
NP_001265441.1:p.Leu858=
|
|
NM_004644.5:c.2515C>T
(AP3B2)
|
NP_004635.2:p.Leu839=
|
|
NM_001278511.2:c.2419C>T
(AP3B2)
|
NP_001265440.1:p.Leu807=
|
|