ENST00000269373.11:c.*229_*237delinsGGGATGTAT
MANE Select
|
ENSP00000269373.6:n.*229_*237delinsGGGATGTAT
|
|
ENST00000269373.10:c.*229_*237delinsGGGATGTAT
|
ENSP00000269373.6:n.*229_*237delinsGGGATGTAT
|
|
ENST00000571594.1:c.53+233_53+241delinsGGGATGTAT
|
ENSP00000459751.1:n.53+233_53+241delinsGGGATGTAT
|
|
ENST00000574832.5:c.*1116_*1124delinsGGGATGTAT
|
ENSP00000460869.1:n.*1116_*1124delinsGGGATGTAT
|
|
NM_024619.3:c.*229_*237delinsGGGATGTAT
|
NP_078895.2:n.*229_*237delinsGGGATGTAT
|
|
NR_046408.1:n.1337_1345delinsGGGATGTAT
|
|
|
XM_024450948.1:c.*229_*237delinsGGGATGTAT
|
XP_024306716.1:n.*229_*237delinsGGGATGTAT
|
|
NM_024619.4:c.*229_*237delinsGGGATGTAT
MANE Select
|
NP_078895.2:n.*229_*237delinsGGGATGTAT
|
|
NR_046408.2:n.1337_1345delinsGGGATGTAT
|
|
|