ENST00000274576.9:c.1053T>C
MANE Select
|
ENSP00000274576.5:p.His351=
|
|
ENST00000274576.8:c.1053T>C
|
ENSP00000274576.4:p.His351=
|
|
ENST00000455880.2:c.1053T>C
|
ENSP00000411593.2:p.His351=
|
|
ENST00000462581.6:c.*811T>C
|
ENSP00000430595.1:n.*811T>C
|
|
NM_000171.3:c.1053T>C
|
NP_000162.2:p.His351=
|
|
NM_001146040.1:c.1053T>C
|
NP_001139512.1:p.His351=
|
|
NM_001292000.1:c.804T>C
|
NP_001278929.1:p.His268=
|
|
NM_000171.4:c.1053T>C
MANE Select
|
NP_000162.2:p.His351=
|
|
NM_001146040.2:c.1053T>C
|
NP_001139512.1:p.His351=
|
|
NM_001292000.2:c.804T>C
|
NP_001278929.1:p.His268=
|
|