|
ENST00000620350.5:c.1245_1248dup
MANE Select
|
ENSP00000484634.1:p.Glu417ThrfsTer6
|
|
|
ENST00000250173.5:c.*109_*112dup
|
ENSP00000250173.2:n.*109_*112dup
|
|
|
ENST00000518642.5:c.*109_*112dup
|
ENSP00000428610.1:n.*109_*112dup
|
|
|
ENST00000519595.5:c.1245_1248dup
|
ENSP00000429791.1:p.Glu417ThrfsTer6
|
|
|
ENST00000522597.1:n.514_517dup
|
|
|
|
ENST00000522789.5:c.465_468dup
|
ENSP00000428015.1:p.Glu157ThrfsTer6
|
|
|
ENST00000618342.1:c.1245_1248dup
|
ENSP00000484802.1:p.Glu417ThrfsTer6
|
|
|
ENST00000620350.4:c.1245_1248dup
|
ENSP00000484634.1:p.Glu417ThrfsTer6
|
|
|
NM_012472.4:c.1245_1248dup
|
NP_036604.2:p.Glu417ThrfsTer6
|
|
|
NR_073525.1:n.1469_1472dup
|
|
|
|
XM_006716538.2:c.1263_1266dup
|
XP_006716601.2:p.Glu423ThrfsTer6
|
|
|
XM_011516950.1:c.1203_1206dup
|
XP_011515252.1:p.Glu403ThrfsTer6
|
|
|
XM_011516952.1:c.999_1002dup
|
XP_011515254.1:p.Glu335ThrfsTer6
|
|
|
XM_011516953.1:c.885_888dup
|
XP_011515255.1:p.Glu297ThrfsTer6
|
|
|
XM_011516954.1:c.885_888dup
|
XP_011515256.1:p.Glu297ThrfsTer6
|
|
|
XR_428377.2:n.1497_1500dup
|
|
|
|
NM_001321961.1:c.1185_1188dup
|
NP_001308890.1:p.Glu397ThrfsTer6
|
|
|
NM_001321962.1:c.999_1002dup
|
NP_001308891.1:p.Glu335ThrfsTer6
|
|
|
NM_001321963.1:c.885_888dup
|
NP_001308892.1:p.Glu297ThrfsTer6
|
|
|
NM_001321964.1:c.885_888dup
|
NP_001308893.1:p.Glu297ThrfsTer6
|
|
|
NM_001321965.1:c.885_888dup
|
NP_001308894.1:p.Glu297ThrfsTer6
|
|
|
NM_001321966.1:c.825_828dup
|
NP_001308895.1:p.Glu277ThrfsTer6
|
|
|
NM_012472.5:c.1245_1248dup
|
NP_036604.2:p.Glu417ThrfsTer6
|
|
|
NR_073525.2:n.1469_1472dup
|
|
|
|
NR_135905.1:n.1458_1461dup
|
|
|
|
NR_135906.1:n.899_902dup
|
|
|
|
NR_135907.1:n.1145_1148dup
|
|
|
|
NR_135908.1:n.839_842dup
|
|
|
|
NR_135909.1:n.1263_1266dup
|
|
|
|
NR_135910.1:n.1570_1573dup
|
|
|
|
NR_135911.1:n.1649_1652dup
|
|
|
|
NR_135912.1:n.2208_2211dup
|
|
|
|
NR_135913.1:n.1895_1898dup
|
|
|
|
XM_006716538.3:c.1263_1266dup
|
XP_006716601.2:p.Glu423ThrfsTer6
|
|
|
XM_011516950.2:c.1203_1206dup
|
XP_011515252.1:p.Glu403ThrfsTer6
|
|
|
XM_017013296.1:c.1143_1146dup
|
XP_016868785.1:p.Glu383ThrfsTer6
|
|
|
XM_017013297.1:c.885_888dup
|
XP_016868786.1:p.Glu297ThrfsTer6
|
|
|
XM_017013298.1:c.885_888dup
|
XP_016868787.1:p.Glu297ThrfsTer6
|
|
|
NM_012472.6:c.1245_1248dup
MANE Select
|
NP_036604.2:p.Glu417ThrfsTer6
|
|
|
NM_001321961.2:c.1185_1188dup
|
NP_001308890.1:p.Glu397ThrfsTer6
|
|
|
NM_001321962.2:c.999_1002dup
|
NP_001308891.1:p.Glu335ThrfsTer6
|
|
|
NM_001321963.2:c.885_888dup
|
NP_001308892.1:p.Glu297ThrfsTer6
|
|
|
NM_001321964.2:c.885_888dup
|
NP_001308893.1:p.Glu297ThrfsTer6
|
|
|
NM_001321965.2:c.885_888dup
|
NP_001308894.1:p.Glu297ThrfsTer6
|
|
|
NM_001321966.2:c.825_828dup
|
NP_001308895.1:p.Glu277ThrfsTer6
|
|
|
NR_073525.3:n.1397_1400dup
|
|
|
|
NR_135905.2:n.1386_1389dup
|
|
|
|
NR_135906.2:n.827_830dup
|
|
|
|
NR_135907.2:n.1073_1076dup
|
|
|
|
NR_135908.2:n.767_770dup
|
|
|
|
NR_135909.2:n.1283_1286dup
|
|
|
|
NR_135910.2:n.1633_1636dup
|
|
|
|
NR_135911.2:n.1753_1756dup
|
|
|
|
NR_135912.2:n.2312_2315dup
|
|
|
|
NR_135913.2:n.1999_2002dup
|
|
|
