|
ENST00000435180.6:c.760A>C
|
ENSP00000391168.2:n.760A>C
|
|
|
ENST00000607071.6:c.*1268A>C
|
ENSP00000475855.1:n.*1268A>C
|
|
|
ENST00000642244.1:c.1458A>C
|
ENSP00000493554.1:p.Glu486Asp
|
|
|
ENST00000642903.1:c.1548A>C
|
ENSP00000493559.1:p.Glu516Asp
|
|
|
ENST00000644972.1:c.1548A>C
|
ENSP00000496451.1:p.Glu516Asp
|
|
|
ENST00000645077.1:c.*1169A>C
|
ENSP00000496113.1:n.*1169A>C
|
|
|
ENST00000645172.1:c.*1250A>C
|
ENSP00000495367.1:n.*1250A>C
|
|
|
ENST00000646190.1:n.2879A>C
|
|
|
|
ENST00000646208.1:c.1284A>C
|
ENSP00000493723.1:p.Glu428Asp
|
|
|
ENST00000646410.1:c.1419A>C
|
ENSP00000494205.1:p.Glu473Asp
|
|
|
ENST00000646562.1:c.*1382A>C
|
ENSP00000496087.1:n.*1382A>C
|
|
|
ENST00000647468.2:c.1548A>C
MANE Select
|
ENSP00000496731.1:p.Glu516Asp
|
|
|
ENST00000648111.1:c.*1236A>C
|
ENSP00000497275.1:n.*1236A>C
|
|
|
ENST00000367101.5:c.1592A>C
|
ENSP00000356068.1:p.Lys531Thr
|
|
|
ENST00000367104.7:c.1548A>C
|
ENSP00000356071.3:p.Glu516Asp
|
|
|
ENST00000435180.5:c.273A>C
|
ENSP00000391168.1:p.Glu91Asp
|
|
|
ENST00000606965.5:c.*109A>C
|
ENSP00000475808.1:n.*109A>C
|
|
|
ENST00000607071.5:c.*1482A>C
|
ENSP00000475855.1:n.*1482A>C
|
|
|
ENST00000607742.5:c.*2826A>C
|
ENSP00000475523.1:n.*2826A>C
|
|
|
NM_032861.3:c.1548A>C
|
NP_116250.3:p.Glu516Asp
|
|
|
NR_073096.1:n.1481A>C
|
|
|
|
XM_006715586.1:c.1338A>C
|
XP_006715649.1:p.Glu446Asp
|
|
|
XM_011536196.1:c.1527A>C
|
XP_011534498.1:p.Glu509Asp
|
|
|
XM_011536197.1:c.1434A>C
|
XP_011534499.1:p.Glu478Asp
|
|
|
XM_011536198.1:c.1338A>C
|
XP_011534500.1:p.Glu446Asp
|
|
|
XM_006715586.3:c.1338A>C
|
XP_006715649.1:p.Glu446Asp
|
|
|
XM_011536196.3:c.1527A>C
|
XP_011534498.1:p.Glu509Asp
|
|
|
XM_011536198.3:c.1338A>C
|
XP_011534500.1:p.Glu446Asp
|
|
|
XM_024446573.1:c.1548A>C
|
XP_024302341.1:p.Glu516Asp
|
|
|
XR_001743697.2:n.1579A>C
|
|
|
|
XR_942606.2:n.1630A>C
|
|
|
|
NM_032861.4:c.1548A>C
MANE Select
|
NP_116250.3:p.Glu516Asp
|
|
|
NR_073096.2:n.1463A>C
|
|
|
