|
ENST00000435180.6:c.819G>T
|
ENSP00000391168.2:n.819G>T
|
|
|
ENST00000607071.6:c.*1327G>T
|
ENSP00000475855.1:n.*1327G>T
|
|
|
ENST00000642244.1:c.1517G>T
|
ENSP00000493554.1:p.Gly506Val
|
|
|
ENST00000642903.1:c.1607G>T
|
ENSP00000493559.1:p.Gly536Val
|
|
|
ENST00000644972.1:c.1607G>T
|
ENSP00000496451.1:p.Gly536Val
|
|
|
ENST00000645077.1:c.*1228G>T
|
ENSP00000496113.1:n.*1228G>T
|
|
|
ENST00000645172.1:c.*1309G>T
|
ENSP00000495367.1:n.*1309G>T
|
|
|
ENST00000646190.1:n.2938G>T
|
|
|
|
ENST00000646208.1:c.1343G>T
|
ENSP00000493723.1:p.Gly448Val
|
|
|
ENST00000646410.1:c.1478G>T
|
ENSP00000494205.1:p.Gly493Val
|
|
|
ENST00000646562.1:c.*1441G>T
|
ENSP00000496087.1:n.*1441G>T
|
|
|
ENST00000647468.2:c.1607G>T
MANE Select
|
ENSP00000496731.1:p.Gly536Val
|
|
|
ENST00000648111.1:c.*1295G>T
|
ENSP00000497275.1:n.*1295G>T
|
|
|
ENST00000367101.5:c.*55G>T
|
ENSP00000356068.1:n.*55G>T
|
|
|
ENST00000367104.7:c.1607G>T
|
ENSP00000356071.3:p.Gly536Val
|
|
|
ENST00000435180.5:c.332G>T
|
ENSP00000391168.1:p.Gly111Val
|
|
|
ENST00000606965.5:c.*168G>T
|
ENSP00000475808.1:n.*168G>T
|
|
|
ENST00000607071.5:c.*1541G>T
|
ENSP00000475855.1:n.*1541G>T
|
|
|
ENST00000607742.5:c.*2885G>T
|
ENSP00000475523.1:n.*2885G>T
|
|
|
NM_032861.3:c.1607G>T
|
NP_116250.3:p.Gly536Val
|
|
|
NR_073096.1:n.1540G>T
|
|
|
|
XM_006715586.1:c.1397G>T
|
XP_006715649.1:p.Gly466Val
|
|
|
XM_011536196.1:c.1586G>T
|
XP_011534498.1:p.Gly529Val
|
|
|
XM_011536197.1:c.1493G>T
|
XP_011534499.1:p.Gly498Val
|
|
|
XM_011536198.1:c.1397G>T
|
XP_011534500.1:p.Gly466Val
|
|
|
XM_006715586.3:c.1397G>T
|
XP_006715649.1:p.Gly466Val
|
|
|
XM_011536196.3:c.1586G>T
|
XP_011534498.1:p.Gly529Val
|
|
|
XM_011536198.3:c.1397G>T
|
XP_011534500.1:p.Gly466Val
|
|
|
XM_024446573.1:c.1607G>T
|
XP_024302341.1:p.Gly536Val
|
|
|
XR_001743697.2:n.1638G>T
|
|
|
|
XR_942606.2:n.1689G>T
|
|
|
|
NM_032861.4:c.1607G>T
MANE Select
|
NP_116250.3:p.Gly536Val
|
|
|
NR_073096.2:n.1522G>T
|
|
|
