ENST00000340855.11:c.669T>G
MANE Select
|
ENSP00000339801.6:p.Val223=
|
|
ENST00000651111.1:c.36T>G
|
ENSP00000498395.1:p.Val12=
|
|
ENST00000340855.10:c.669T>G
|
ENSP00000339801.6:p.Val223=
|
|
ENST00000370441.8:c.669T>G
|
ENSP00000359470.4:p.Val223=
|
|
ENST00000422081.6:c.36T>G
|
ENSP00000477056.1:p.Val12=
|
|
ENST00000441880.1:n.114-11048T>G
|
|
|
ENST00000464251.5:c.595T>G
|
ENSP00000428980.1:n.595T>G
|
|
ENST00000466019.1:n.121T>G
|
|
|
ENST00000466323.5:c.669T>G
|
ENSP00000418264.1:p.Val223=
|
|
ENST00000490775.5:n.454T>G
|
|
|
NM_000202.6:c.669T>G
|
NP_000193.1:p.Val223=
|
|
NM_001166550.2:c.399T>G
|
NP_001160022.1:p.Val133=
|
|
NM_006123.4:c.669T>G
|
NP_006114.1:p.Val223=
|
|
NR_104128.1:n.886T>G
|
|
|
NM_000202.7:c.669T>G
|
NP_000193.1:p.Val223=
|
|
NM_001166550.3:c.399T>G
|
NP_001160022.1:p.Val133=
|
|
NM_000202.8:c.669T>G
MANE Select
|
NP_000193.1:p.Val223=
|
|
NM_001166550.4:c.399T>G
|
NP_001160022.1:p.Val133=
|
|
NM_006123.5:c.669T>G
|
NP_006114.1:p.Val223=
|
|
NR_104128.2:n.838T>G
|
|
|