ENST00000274576.9:c.*43G>A
MANE Select
|
ENSP00000274576.5:n.*43G>A
|
|
ENST00000274576.8:c.*43G>A
|
ENSP00000274576.4:n.*43G>A
|
|
ENST00000455880.2:c.*43G>A
|
ENSP00000411593.2:n.*43G>A
|
|
ENST00000462581.6:c.*1151G>A
|
ENSP00000430595.1:n.*1151G>A
|
|
NM_000171.3:c.*43G>A
|
NP_000162.2:n.*43G>A
|
|
NM_001146040.1:c.*43G>A
|
NP_001139512.1:n.*43G>A
|
|
NM_001292000.1:c.*43G>A
|
NP_001278929.1:n.*43G>A
|
|
NM_000171.4:c.*43G>A
MANE Select
|
NP_000162.2:n.*43G>A
|
|
NM_001146040.2:c.*43G>A
|
NP_001139512.1:n.*43G>A
|
|
NM_001292000.2:c.*43G>A
|
NP_001278929.1:n.*43G>A
|
|