ENST00000269373.11:c.*765_*767delinsGAC
MANE Select
|
ENSP00000269373.6:n.*765_*767delinsGAC
|
|
ENST00000269373.10:c.*765_*767delinsGAC
|
ENSP00000269373.6:n.*765_*767delinsGAC
|
|
ENST00000571594.1:c.53+769_53+771delinsGAC
|
ENSP00000459751.1:n.53+769_53+771delinsGAC
|
|
NM_024619.3:c.*765_*767delinsGAC
|
NP_078895.2:n.*765_*767delinsGAC
|
|
NR_046408.1:n.1873_1875delinsGAC
|
|
|
XM_024450948.1:c.*765_*767delinsGAC
|
XP_024306716.1:n.*765_*767delinsGAC
|
|
NM_024619.4:c.*765_*767delinsGAC
MANE Select
|
NP_078895.2:n.*765_*767delinsGAC
|
|
NR_046408.2:n.1873_1875delinsGAC
|
|
|