ENST00000689792.1:n.1369_1373delinsGGAGA
|
|
|
ENST00000262948.10:c.*262_*266delinsGGAGA
MANE Select
|
ENSP00000262948.4:n.*262_*266delinsGGAGA
|
|
ENST00000262948.9:c.*262_*266delinsGGAGA
|
ENSP00000262948.3:n.*262_*266delinsGGAGA
|
|
ENST00000600584.5:n.2914_2918delinsGGAGA
|
|
|
ENST00000601786.5:n.1766_1770delinsGGAGA
|
|
|
NM_030662.3:c.*262_*266delinsGGAGA , LRG_750t1:c.*262_*266delinsGGAGA
|
NP_109587.1:n.*262_*266delinsGGAGA
|
|
XM_006722799.2:c.*262_*266delinsGGAGA
|
XP_006722862.1:n.*262_*266delinsGGAGA
|
|
XM_011528133.1:c.*262_*266delinsGGAGA
|
XP_011526435.1:n.*262_*266delinsGGAGA
|
|
NM_030662.4:c.*262_*266delinsGGAGA
MANE Select
|
NP_109587.1:n.*262_*266delinsGGAGA
|
|