|
ENST00000261722.8:c.2882C>T
(AP3B2)
|
ENSP00000261722.4:p.Thr961Ile
|
|
|
ENST00000535359.6:c.2921C>T
(AP3B2)
MANE Select
|
ENSP00000440984.1:p.Thr974Ile
|
|
|
ENST00000535385.6:n.3808C>T
(AP3B2)
|
|
|
|
ENST00000537735.2:n.3010C>T
(AP3B2)
|
|
|
|
ENST00000543938.6:n.3508C>T
(AP3B2)
|
|
|
|
ENST00000642989.2:c.2993C>T
(AP3B2)
|
ENSP00000493485.1:p.Thr998Ile
|
|
|
ENST00000652847.1:c.2864C>T
(AP3B2)
|
ENSP00000499785.1:p.Thr955Ile
|
|
|
ENST00000657321.1:c.*2710C>T
(AP3B2)
|
ENSP00000499716.1:n.*2710C>T
|
|
|
ENST00000660624.1:c.1772C>T
(AP3B2)
|
ENSP00000499379.1:p.Thr591Ile
|
|
|
ENST00000661532.1:c.2153C>T
(AP3B2)
|
|
|
|
ENST00000663651.1:n.3006C>T
(AP3B2)
|
|
|
|
ENST00000666973.1:c.2864C>T
(AP3B2)
|
ENSP00000499288.1:p.Thr955Ile
|
|
|
ENST00000667758.1:c.*3519C>T
(AP3B2)
|
ENSP00000499318.1:n.*3519C>T
|
|
|
ENST00000668385.1:c.*2662C>T
(AP3B2)
|
ENSP00000499544.1:n.*2662C>T
|
|
|
ENST00000668458.1:c.2612C>T
(AP3B2)
|
|
|
|
ENST00000668990.2:c.2864C>T
(AP3B2)
|
ENSP00000499235.1:p.Thr955Ile
|
|
|
ENST00000669930.1:c.2693C>T
(AP3B2)
|
ENSP00000499671.1:p.Thr898Ile
|
|
|
ENST00000679388.1:n.3448C>T
(AP3B2)
|
|
|
|
ENST00000679531.1:n.3711C>T
(AP3B2)
|
|
|
|
ENST00000679891.1:n.1742C>T
(AP3B2)
|
|
|
|
ENST00000679950.1:n.4010C>T
(AP3B2)
|
|
|
|
ENST00000680492.1:n.4344C>T
(AP3B2)
|
|
|
|
ENST00000680912.1:n.2281C>T
(AP3B2)
|
|
|
|
ENST00000680946.1:n.3915C>T
(AP3B2)
|
|
|
|
ENST00000681044.1:n.4421C>T
(AP3B2)
|
|
|
|
ENST00000681327.1:c.*2710C>T
(AP3B2)
|
ENSP00000505423.1:n.*2710C>T
|
|
|
ENST00000681452.1:n.3270C>T
(AP3B2)
|
|
|
|
ENST00000681464.1:n.4217C>T
(AP3B2)
|
|
|
|
ENST00000261722.7:c.2864C>T
(AP3B2)
|
ENSP00000261722.3:p.Thr955Ile
|
|
|
ENST00000535348.5:c.2768C>T
(AP3B2)
|
ENSP00000438721.1:p.Thr923Ile
|
|
|
ENST00000535359.5:c.2921C>T
(AP3B2)
|
ENSP00000440984.1:p.Thr974Ile
|
|
|
ENST00000537735.1:n.532C>T
(AP3B2)
|
|
|
|
ENST00000543938.5:n.1987C>T
(AP3B2)
|
|
|
|
ENST00000620652.4:c.2864C>T
(AP3B2)
|
ENSP00000479229.1:p.Thr955Ile
|
|
|
NM_001278511.1:c.2768C>T
(AP3B2)
|
NP_001265440.1:p.Thr923Ile
|
|
|
NM_001278512.1:c.2921C>T
(AP3B2)
|
NP_001265441.1:p.Thr974Ile
|
|
|
NM_004644.4:c.2864C>T
(AP3B2)
|
NP_004635.2:p.Thr955Ile
|
|
|
NR_046096.1:n.1328+11774G>A
(CPEB1-AS1)
|
|
|
|
XM_011522097.1:c.2849C>T
(AP3B2)
|
XP_011520399.1:p.Thr950Ile
|
|
|
XM_011522098.1:c.2825C>T
(AP3B2)
|
XP_011520400.1:p.Thr942Ile
|
|
|
XM_011522100.1:c.1772C>T
(AP3B2)
|
XP_011520402.1:p.Thr591Ile
|
|
|
NM_001348441.1:c.53C>T
(AP3B2)
|
NP_001335370.1:p.Thr18Ile
|
|
|
XM_017022640.2:c.2792C>T
(AP3B2)
|
XP_016878129.1:p.Thr931Ile
|
|
|
XM_024450081.1:c.203C>T
(AP3B2)
|
XP_024305849.1:p.Thr68Ile
|
|
|
XM_024450082.1:c.53C>T
(AP3B2)
|
XP_024305850.1:p.Thr18Ile
|
|
|
XR_001751404.2:n.3092C>T
(AP3B2)
|
|
|
|
NM_001278512.2:c.2921C>T
(AP3B2)
MANE Select
|
NP_001265441.1:p.Thr974Ile
|
|
|
NM_004644.5:c.2864C>T
(AP3B2)
|
NP_004635.2:p.Thr955Ile
|
|
|
NM_001278511.2:c.2768C>T
(AP3B2)
|
NP_001265440.1:p.Thr923Ile
|
|
|
NM_001348441.2:c.53C>T
(AP3B2)
|
NP_001335370.1:p.Thr18Ile
|
|
