|
NM_000124.4:c.1397+8614G>T
(ERCC6)
MANE Select
|
NP_000115.1:n.1397+8614G>T
|
|
ENST00000355832.10:c.1397+8614G>T
(ERCC6)
MANE Select
|
ENSP00000348089.5:n.1397+8614G>T
|
|
NM_001277058.2:c.3100G>T
(ERCC6)
MANE Plus Clinical
|
NP_001263987.1:p.Glu1034Ter
|
|
ENST00000447839.7:c.3100G>T
(ERCC6)
MANE Plus Clinical
|
ENSP00000387966.2:p.Glu1034Ter
|
|
NM_000124.3:c.1397+8614G>T
(ERCC6)
|
NP_000115.1:n.1397+8614G>T
|
|
NM_001277058.1:c.3100G>T
|
NP_001263987.1:p.Glu1034Ter
|
|
NM_001277059.1:c.3100G>T
|
NP_001263988.1:p.Glu1034Ter
|
|
NM_001277059.2:c.3100G>T
(ERCC6)
|
NP_001263988.1:p.Glu1034Ter
|
|
NM_001346440.1:c.1397+8614G>T
(ERCC6)
|
NP_001333369.1:n.1397+8614G>T
|
|
NM_001346440.2:c.1397+8614G>T
(ERCC6)
|
NP_001333369.1:n.1397+8614G>T
|
|
NM_170753.3:c.1696G>T
(PGBD3)
|
NP_736609.2:p.Glu566Ter
|
|
ENST00000355832.9:c.1397+8614G>T
(ERCC6)
|
ENSP00000348089.5:n.1397+8614G>T
|
|
ENST00000374127.3:c.1696G>T
|
ENSP00000363242.3:p.Glu566Ter
|
|
ENST00000447839.6:c.3100G>T
|
ENSP00000387966.2:p.Glu1034Ter
|
|
ENST00000515869.1:c.3100G>T
|
ENSP00000423550.1:p.Glu1034Ter
|
|
ENST00000679596.1:c.*2729G>T
(ERCC6)
|
ENSP00000504862.1:n.*2729G>T
|
|
ENST00000679811.1:n.1480+8614G>T
(ERCC6)
|
|
|
ENST00000680107.1:c.*1680G>T
(ERCC6)
|
ENSP00000505909.1:n.*1680G>T
|
|
ENST00000681632.1:n.1475+8614G>T
(ERCC6)
|
|
|
ENST00000681659.1:c.1397+8614G>T
(ERCC6)
|
ENSP00000505631.1:n.1397+8614G>T
|
