ENST00000435180.6:c.840_841dup
|
ENSP00000391168.2:n.840_841dup
|
|
ENST00000607071.6:c.*1348_*1349dup
|
ENSP00000475855.1:n.*1348_*1349dup
|
|
ENST00000642244.1:c.1538_1539dup
|
ENSP00000493554.1:p.Val514LeufsTer?
|
|
ENST00000642903.1:c.1628_1629dup
|
ENSP00000493559.1:p.Val544LeufsTer?
|
|
ENST00000644972.1:c.1628_1629dup
|
ENSP00000496451.1:p.Val544LeufsTer?
|
|
ENST00000645077.1:c.*1249_*1250dup
|
ENSP00000496113.1:n.*1249_*1250dup
|
|
ENST00000645172.1:c.*1330_*1331dup
|
ENSP00000495367.1:n.*1330_*1331dup
|
|
ENST00000646190.1:n.2959_2960dup
|
|
|
ENST00000646208.1:c.1364_1365dup
|
ENSP00000493723.1:p.Val456LeufsTer?
|
|
ENST00000646410.1:c.1499_1500dup
|
ENSP00000494205.1:p.Val501LeufsTer?
|
|
ENST00000646562.1:c.*1462_*1463dup
|
ENSP00000496087.1:n.*1462_*1463dup
|
|
ENST00000647468.2:c.1628_1629dup
MANE Select
|
ENSP00000496731.1:p.Val544LeufsTer?
|
|
ENST00000648111.1:c.*1316_*1317dup
|
ENSP00000497275.1:n.*1316_*1317dup
|
|
ENST00000367101.5:c.*76_*77dup
|
ENSP00000356068.1:n.*76_*77dup
|
|
ENST00000367104.7:c.1628_1629dup
|
ENSP00000356071.3:p.Val544LeufsTer?
|
|
ENST00000435180.5:c.353_354dup
|
ENSP00000391168.1:p.Val119LeufsTer?
|
|
ENST00000606965.5:c.*189_*190dup
|
ENSP00000475808.1:n.*189_*190dup
|
|
ENST00000607071.5:c.*1562_*1563dup
|
ENSP00000475855.1:n.*1562_*1563dup
|
|
ENST00000607742.5:c.*2906_*2907dup
|
ENSP00000475523.1:n.*2906_*2907dup
|
|
NM_032861.3:c.1628_1629dup
|
NP_116250.3:p.Val544LeufsTer?
|
|
NR_073096.1:n.1561_1562dup
|
|
|
XM_006715586.1:c.1418_1419dup
|
XP_006715649.1:p.Val474LeufsTer?
|
|
XM_011536196.1:c.1607_1608dup
|
XP_011534498.1:p.Val537LeufsTer?
|
|
XM_011536197.1:c.1514_1515dup
|
XP_011534499.1:p.Val506LeufsTer?
|
|
XM_011536198.1:c.1418_1419dup
|
XP_011534500.1:p.Val474LeufsTer?
|
|
XM_006715586.3:c.1418_1419dup
|
XP_006715649.1:p.Val474LeufsTer?
|
|
XM_011536196.3:c.1607_1608dup
|
XP_011534498.1:p.Val537LeufsTer?
|
|
XM_011536198.3:c.1418_1419dup
|
XP_011534500.1:p.Val474LeufsTer?
|
|
XM_024446573.1:c.1628_1629dup
|
XP_024302341.1:p.Val544LeufsTer?
|
|
XR_001743697.2:n.1659_1660dup
|
|
|
XR_942606.2:n.1710_1711dup
|
|
|
NM_032861.4:c.1628_1629dup
MANE Select
|
NP_116250.3:p.Val544LeufsTer?
|
|
NR_073096.2:n.1543_1544dup
|
|
|