|
ENST00000261722.8:c.2920G>A
(AP3B2)
|
ENSP00000261722.4:p.Val974Ile
|
|
|
ENST00000535359.6:c.2959G>A
(AP3B2)
MANE Select
|
ENSP00000440984.1:p.Val987Ile
|
|
|
ENST00000535385.6:n.3846G>A
(AP3B2)
|
|
|
|
ENST00000537735.2:n.3048G>A
(AP3B2)
|
|
|
|
ENST00000543938.6:n.3546G>A
(AP3B2)
|
|
|
|
ENST00000642989.2:c.3031G>A
(AP3B2)
|
ENSP00000493485.1:p.Val1011Ile
|
|
|
ENST00000652847.1:c.2902G>A
(AP3B2)
|
ENSP00000499785.1:p.Val968Ile
|
|
|
ENST00000657321.1:c.*2748G>A
(AP3B2)
|
ENSP00000499716.1:n.*2748G>A
|
|
|
ENST00000660624.1:c.1810G>A
(AP3B2)
|
ENSP00000499379.1:p.Val604Ile
|
|
|
ENST00000661532.1:c.2191G>A
(AP3B2)
|
|
|
|
ENST00000663651.1:n.3044G>A
(AP3B2)
|
|
|
|
ENST00000666973.1:c.2902G>A
(AP3B2)
|
ENSP00000499288.1:p.Val968Ile
|
|
|
ENST00000667758.1:c.*3557G>A
(AP3B2)
|
ENSP00000499318.1:n.*3557G>A
|
|
|
ENST00000668385.1:c.*2700G>A
(AP3B2)
|
ENSP00000499544.1:n.*2700G>A
|
|
|
ENST00000668458.1:c.2650G>A
(AP3B2)
|
|
|
|
ENST00000668990.2:c.2902G>A
(AP3B2)
|
ENSP00000499235.1:p.Val968Ile
|
|
|
ENST00000669930.1:c.2731G>A
(AP3B2)
|
ENSP00000499671.1:p.Val911Ile
|
|
|
ENST00000679388.1:n.3486G>A
(AP3B2)
|
|
|
|
ENST00000679531.1:n.3749G>A
(AP3B2)
|
|
|
|
ENST00000679891.1:n.1780G>A
(AP3B2)
|
|
|
|
ENST00000679950.1:n.4048G>A
(AP3B2)
|
|
|
|
ENST00000680492.1:n.4382G>A
(AP3B2)
|
|
|
|
ENST00000680912.1:n.2319G>A
(AP3B2)
|
|
|
|
ENST00000680946.1:n.3953G>A
(AP3B2)
|
|
|
|
ENST00000681044.1:n.4459G>A
(AP3B2)
|
|
|
|
ENST00000681327.1:c.*2748G>A
(AP3B2)
|
ENSP00000505423.1:n.*2748G>A
|
|
|
ENST00000681452.1:n.3308G>A
(AP3B2)
|
|
|
|
ENST00000681464.1:n.4255G>A
(AP3B2)
|
|
|
|
ENST00000261722.7:c.2902G>A
(AP3B2)
|
ENSP00000261722.3:p.Val968Ile
|
|
|
ENST00000535348.5:c.2806G>A
(AP3B2)
|
ENSP00000438721.1:p.Val936Ile
|
|
|
ENST00000535359.5:c.2959G>A
(AP3B2)
|
ENSP00000440984.1:p.Val987Ile
|
|
|
ENST00000537735.1:n.570G>A
(AP3B2)
|
|
|
|
ENST00000543938.5:n.2025G>A
(AP3B2)
|
|
|
|
ENST00000620652.4:c.2902G>A
(AP3B2)
|
ENSP00000479229.1:p.Val968Ile
|
|
|
NM_001278511.1:c.2806G>A
(AP3B2)
|
NP_001265440.1:p.Val936Ile
|
|
|
NM_001278512.1:c.2959G>A
(AP3B2)
|
NP_001265441.1:p.Val987Ile
|
|
|
NM_004644.4:c.2902G>A
(AP3B2)
|
NP_004635.2:p.Val968Ile
|
|
|
NR_046096.1:n.1328+11736C>T
(CPEB1-AS1)
|
|
|
|
XM_011522097.1:c.2887G>A
(AP3B2)
|
XP_011520399.1:p.Val963Ile
|
|
|
XM_011522098.1:c.2863G>A
(AP3B2)
|
XP_011520400.1:p.Val955Ile
|
|
|
XM_011522100.1:c.1810G>A
(AP3B2)
|
XP_011520402.1:p.Val604Ile
|
|
|
NM_001348441.1:c.91G>A
(AP3B2)
|
NP_001335370.1:p.Val31Ile
|
|
|
XM_017022640.2:c.2830G>A
(AP3B2)
|
XP_016878129.1:p.Val944Ile
|
|
|
XM_024450081.1:c.241G>A
(AP3B2)
|
XP_024305849.1:p.Val81Ile
|
|
|
XM_024450082.1:c.91G>A
(AP3B2)
|
XP_024305850.1:p.Val31Ile
|
|
|
XR_001751404.2:n.3130G>A
(AP3B2)
|
|
|
|
NM_001278512.2:c.2959G>A
(AP3B2)
MANE Select
|
NP_001265441.1:p.Val987Ile
|
|
|
NM_004644.5:c.2902G>A
(AP3B2)
|
NP_004635.2:p.Val968Ile
|
|
|
NM_001278511.2:c.2806G>A
(AP3B2)
|
NP_001265440.1:p.Val936Ile
|
|
|
NM_001348441.2:c.91G>A
(AP3B2)
|
NP_001335370.1:p.Val31Ile
|
|
