ENST00000340855.11:c.955G=
MANE Select
|
ENSP00000339801.6:p.Asp319=
|
|
ENST00000651111.1:c.322G=
|
ENSP00000498395.1:p.Asp108=
|
|
ENST00000340855.10:c.955G=
|
ENSP00000339801.6:p.Asp319=
|
|
ENST00000370441.8:c.955G=
|
ENSP00000359470.4:p.Asp319=
|
|
ENST00000422081.6:c.322G=
|
ENSP00000477056.1:p.Asp108=
|
|
ENST00000441880.1:n.114-3267G=
|
|
|
ENST00000464251.5:c.881G=
|
ENSP00000428980.1:n.881G=
|
|
ENST00000466323.5:c.*146G=
|
ENSP00000418264.1:n.*146G=
|
|
ENST00000490775.5:n.740G=
|
|
|
NM_000202.6:c.955G=
|
NP_000193.1:p.Asp319=
|
|
NM_001166550.2:c.685G=
|
NP_001160022.1:p.Asp229=
|
|
NM_006123.4:c.955G=
|
NP_006114.1:p.Asp319=
|
|
NR_104128.1:n.1302G=
|
|
|
NM_000202.7:c.955G=
|
NP_000193.1:p.Asp319=
|
|
NM_001166550.3:c.685G=
|
NP_001160022.1:p.Asp229=
|
|
NM_000202.8:c.955G=
MANE Select
|
NP_000193.1:p.Asp319=
|
|
NM_001166550.4:c.685G=
|
NP_001160022.1:p.Asp229=
|
|
NM_006123.5:c.955G=
|
NP_006114.1:p.Asp319=
|
|
NR_104128.2:n.1254G=
|
|
|