|
ENST00000261722.8:c.249C>T
(AP3B2)
|
ENSP00000261722.4:p.Ala83=
|
|
|
ENST00000535359.6:c.249C>T
(AP3B2)
MANE Select
|
ENSP00000440984.1:p.Ala83=
|
|
|
ENST00000535385.6:n.426C>T
(AP3B2)
|
|
|
|
ENST00000535513.2:c.249C>T
(AP3B2)
|
ENSP00000499258.1:p.Ala83=
|
|
|
ENST00000537735.2:n.395C>T
(AP3B2)
|
|
|
|
ENST00000543938.6:n.452C>T
(AP3B2)
|
|
|
|
ENST00000642989.2:c.378C>T
(AP3B2)
|
ENSP00000493485.1:p.Ala126=
|
|
|
ENST00000652847.1:c.249C>T
(AP3B2)
|
ENSP00000499785.1:p.Ala83=
|
|
|
ENST00000657321.1:c.249C>T
(AP3B2)
|
ENSP00000499716.1:p.Ala83=
|
|
|
ENST00000663651.1:n.391C>T
(AP3B2)
|
|
|
|
ENST00000664460.1:c.249C>T
(AP3B2)
|
ENSP00000499798.1:p.Ala83=
|
|
|
ENST00000666055.1:c.249C>T
(AP3B2)
|
ENSP00000499608.1:p.Ala83=
|
|
|
ENST00000666973.1:c.249C>T
(AP3B2)
|
ENSP00000499288.1:p.Ala83=
|
|
|
ENST00000667758.1:c.249C>T
(AP3B2)
|
ENSP00000499318.1:p.Ala83=
|
|
|
ENST00000668385.1:c.190-61C>T
(AP3B2)
|
ENSP00000499544.1:n.190-61C>T
|
|
|
ENST00000668990.2:c.249C>T
(AP3B2)
|
ENSP00000499235.1:p.Ala83=
|
|
|
ENST00000669930.1:c.189+205C>T
(AP3B2)
|
ENSP00000499671.1:n.189+205C>T
|
|
|
ENST00000679388.1:n.188C>T
(AP3B2)
|
|
|
|
ENST00000679531.1:n.655C>T
(AP3B2)
|
|
|
|
ENST00000679950.1:n.458C>T
(AP3B2)
|
|
|
|
ENST00000680492.1:n.655C>T
(AP3B2)
|
|
|
|
ENST00000680946.1:n.655C>T
(AP3B2)
|
|
|
|
ENST00000681044.1:n.655C>T
(AP3B2)
|
|
|
|
ENST00000681327.1:c.249C>T
(AP3B2)
|
ENSP00000505423.1:p.Ala83=
|
|
|
ENST00000681452.1:n.655C>T
(AP3B2)
|
|
|
|
ENST00000681464.1:n.655C>T
(AP3B2)
|
|
|
|
ENST00000261722.7:c.249C>T
(AP3B2)
|
ENSP00000261722.3:p.Ala83=
|
|
|
ENST00000535348.5:c.249C>T
(AP3B2)
|
ENSP00000438721.1:p.Ala83=
|
|
|
ENST00000535359.5:c.249C>T
(AP3B2)
|
ENSP00000440984.1:p.Ala83=
|
|
|
ENST00000535385.5:n.426C>T
(AP3B2)
|
|
|
|
ENST00000535513.1:n.416C>T
(AP3B2)
|
|
|
|
ENST00000541693.5:c.117C>T
(AP3B2)
|
ENSP00000441961.1:p.Ala39=
|
|
|
ENST00000542200.2:c.249C>T
(AP3B2)
|
ENSP00000440719.1:p.Ala83=
|
|
|
ENST00000561455.5:n.216C>T
(AP3B2)
|
|
|
|
ENST00000620652.4:c.249C>T
(AP3B2)
|
ENSP00000479229.1:p.Ala83=
|
|
|
NM_001278511.1:c.249C>T
(AP3B2)
|
NP_001265440.1:p.Ala83=
|
|
|
NM_001278512.1:c.249C>T
(AP3B2)
|
NP_001265441.1:p.Ala83=
|
|
|
NM_004644.4:c.249C>T
(AP3B2)
|
NP_004635.2:p.Ala83=
|
|
|
NR_046096.1:n.1329-2838G>A
(CPEB1-AS1)
|
|
|
|
XM_011522097.1:c.249C>T
(AP3B2)
|
XP_011520399.1:p.Ala83=
|
|
|
XM_011522098.1:c.249C>T
(AP3B2)
|
XP_011520400.1:p.Ala83=
|
|
|
XM_011522099.1:c.249C>T
(AP3B2)
|
XP_011520401.1:p.Ala83=
|
|
|
NM_001348440.1:c.249C>T
(AP3B2)
|
NP_001335369.1:p.Ala83=
|
|
|
XM_017022640.2:c.249C>T
(AP3B2)
|
XP_016878129.1:p.Ala83=
|
|
|
XM_017022641.2:c.249C>T
(AP3B2)
|
XP_016878130.1:p.Ala83=
|
|
|
XR_001751404.2:n.415C>T
(AP3B2)
|
|
|
|
NM_001278512.2:c.249C>T
(AP3B2)
MANE Select
|
NP_001265441.1:p.Ala83=
|
|
|
NM_004644.5:c.249C>T
(AP3B2)
|
NP_004635.2:p.Ala83=
|
|
|
NM_001278511.2:c.249C>T
(AP3B2)
|
NP_001265440.1:p.Ala83=
|
|
|
NM_001348440.2:c.249C>T
(AP3B2)
|
NP_001335369.1:p.Ala83=
|
|
