ENST00000340855.11:c.697A>C
MANE Select
|
ENSP00000339801.6:p.Arg233=
|
|
ENST00000651111.1:c.64A>C
|
ENSP00000498395.1:p.Arg22=
|
|
ENST00000340855.10:c.697A>C
|
ENSP00000339801.6:p.Arg233=
|
|
ENST00000370441.8:c.697A>C
|
ENSP00000359470.4:p.Arg233=
|
|
ENST00000422081.6:c.64A>C
|
ENSP00000477056.1:p.Arg22=
|
|
ENST00000441880.1:n.114-11020A>C
|
|
|
ENST00000464251.5:c.623A>C
|
ENSP00000428980.1:n.623A>C
|
|
ENST00000466019.1:n.149A>C
|
|
|
ENST00000466323.5:c.697A>C
|
ENSP00000418264.1:p.Arg233=
|
|
ENST00000490775.5:n.482A>C
|
|
|
NM_000202.6:c.697A>C
|
NP_000193.1:p.Arg233=
|
|
NM_001166550.2:c.427A>C
|
NP_001160022.1:p.Arg143=
|
|
NM_006123.4:c.697A>C
|
NP_006114.1:p.Arg233=
|
|
NR_104128.1:n.914A>C
|
|
|
NM_000202.7:c.697A>C
|
NP_000193.1:p.Arg233=
|
|
NM_001166550.3:c.427A>C
|
NP_001160022.1:p.Arg143=
|
|
NM_000202.8:c.697A>C
MANE Select
|
NP_000193.1:p.Arg233=
|
|
NM_001166550.4:c.427A>C
|
NP_001160022.1:p.Arg143=
|
|
NM_006123.5:c.697A>C
|
NP_006114.1:p.Arg233=
|
|
NR_104128.2:n.866A>C
|
|
|