ENST00000340855.11:c.982A>T
MANE Select
|
ENSP00000339801.6:p.Ile328Phe
|
|
ENST00000651111.1:c.349A>T
|
ENSP00000498395.1:p.Ile117Phe
|
|
ENST00000340855.10:c.982A>T
|
ENSP00000339801.6:p.Ile328Phe
|
|
ENST00000370441.8:c.982A>T
|
ENSP00000359470.4:p.Ile328Phe
|
|
ENST00000422081.6:c.349A>T
|
ENSP00000477056.1:p.Ile117Phe
|
|
ENST00000441880.1:n.114-3240A>T
|
|
|
ENST00000464251.5:c.908A>T
|
ENSP00000428980.1:n.908A>T
|
|
ENST00000466323.5:c.*173A>T
|
ENSP00000418264.1:n.*173A>T
|
|
ENST00000490775.5:n.767A>T
|
|
|
NM_000202.6:c.982A>T
|
NP_000193.1:p.Ile328Phe
|
|
NM_001166550.2:c.712A>T
|
NP_001160022.1:p.Ile238Phe
|
|
NM_006123.4:c.982A>T
|
NP_006114.1:p.Ile328Phe
|
|
NR_104128.1:n.1329A>T
|
|
|
NM_000202.7:c.982A>T
|
NP_000193.1:p.Ile328Phe
|
|
NM_001166550.3:c.712A>T
|
NP_001160022.1:p.Ile238Phe
|
|
NM_000202.8:c.982A>T
MANE Select
|
NP_000193.1:p.Ile328Phe
|
|
NM_001166550.4:c.712A>T
|
NP_001160022.1:p.Ile238Phe
|
|
NM_006123.5:c.982A>T
|
NP_006114.1:p.Ile328Phe
|
|
NR_104128.2:n.1281A>T
|
|
|