ENST00000286648.10:c.*1181_*1183delinsCTG
MANE Select
|
ENSP00000286648.5:n.*1181_*1183delinsCTG
|
|
ENST00000286648.9:c.*1181_*1183delinsCTG
|
ENSP00000286648.5:n.*1181_*1183delinsCTG
|
|
ENST00000503359.5:c.*1908_*1910delinsCTG
|
ENSP00000426389.1:n.*1908_*1910delinsCTG
|
|
ENST00000504730.5:c.*1248_*1250delinsCTG
|
ENSP00000425578.1:n.*1248_*1250delinsCTG
|
|
ENST00000504952.1:c.*1107_*1109delinsCTG
|
ENSP00000421508.1:n.*1107_*1109delinsCTG
|
|
NM_000788.2:c.*1181_*1183delinsCTG
|
NP_000779.1:n.*1181_*1183delinsCTG
|
|
NM_000788.3:c.*1181_*1183delinsCTG
MANE Select
|
NP_000779.1:n.*1181_*1183delinsCTG
|
|