ENST00000340855.11:c.919T>G
MANE Select
|
ENSP00000339801.6:p.Leu307Val
|
|
ENST00000651111.1:c.286T>G
|
ENSP00000498395.1:p.Leu96Val
|
|
ENST00000340855.10:c.919T>G
|
ENSP00000339801.6:p.Leu307Val
|
|
ENST00000370441.8:c.919T>G
|
ENSP00000359470.4:p.Leu307Val
|
|
ENST00000422081.6:c.286T>G
|
ENSP00000477056.1:p.Leu96Val
|
|
ENST00000441880.1:n.114-3303T>G
|
|
|
ENST00000464251.5:c.845T>G
|
ENSP00000428980.1:n.845T>G
|
|
ENST00000466323.5:c.*110T>G
|
ENSP00000418264.1:n.*110T>G
|
|
ENST00000490775.5:n.704T>G
|
|
|
NM_000202.6:c.919T>G
|
NP_000193.1:p.Leu307Val
|
|
NM_001166550.2:c.649T>G
|
NP_001160022.1:p.Leu217Val
|
|
NM_006123.4:c.919T>G
|
NP_006114.1:p.Leu307Val
|
|
NR_104128.1:n.1266T>G
|
|
|
NM_000202.7:c.919T>G
|
NP_000193.1:p.Leu307Val
|
|
NM_001166550.3:c.649T>G
|
NP_001160022.1:p.Leu217Val
|
|
NM_000202.8:c.919T>G
MANE Select
|
NP_000193.1:p.Leu307Val
|
|
NM_001166550.4:c.649T>G
|
NP_001160022.1:p.Leu217Val
|
|
NM_006123.5:c.919T>G
|
NP_006114.1:p.Leu307Val
|
|
NR_104128.2:n.1218T>G
|
|
|