ENST00000407010.7:c.*3261_*3269delinsG
MANE Select
|
ENSP00000385478.2:n.*3261_*3269delinsG
|
|
ENST00000407010.6:c.4617_4625delinsG
|
ENSP00000385478.2:n.4617_4625delinsG
|
|
NM_001101417.3:c.4467_4475delinsG
|
NP_001094887.1:n.4467_4475delinsG
|
|
NM_001101426.3:c.4617_4625delinsG
|
NP_001094896.1:n.4617_4625delinsG
|
|
XM_011515498.1:c.1251+127632_1251+127640delinsG
|
XP_011513800.1:n.1251+127632_1251+127640delinsG
|
|
NM_001101426.4:c.*3261_*3269delinsG
MANE Select
|
NP_001094896.1:n.*3261_*3269delinsG
|
|
NM_001101417.4:c.*3261_*3269delinsG
|
NP_001094887.1:n.*3261_*3269delinsG
|
|
NM_001368197.1:c.*3261_*3269delinsG
|
NP_001355126.1:n.*3261_*3269delinsG
|
|
NR_160656.1:n.4682_4690delinsG
|
|
|