ENST00000378364.8:c.364A>C
MANE Select
|
ENSP00000367615.3:p.Arg122=
|
|
ENST00000378364.7:c.364A>C
|
ENSP00000367615.3:p.Arg122=
|
|
ENST00000426324.6:c.364A>C
|
ENSP00000397007.2:p.Arg122=
|
|
ENST00000562464.1:n.374A>C
|
|
|
ENST00000563655.5:c.283A>C
|
ENSP00000456012.1:p.Arg95=
|
|
ENST00000567057.5:n.163A>C
|
|
|
ENST00000567391.5:c.*38A>C
|
ENSP00000457964.1:n.*38A>C
|
|
ENST00000567713.5:c.321+317A>C
|
ENSP00000455749.1:n.321+317A>C
|
|
ENST00000568319.5:c.*38A>C
|
ENSP00000456905.1:n.*38A>C
|
|
ENST00000568575.1:n.293A>C
|
|
|
ENST00000569616.1:c.362A>C
|
|
|
NM_000485.2:c.364A>C
|
NP_000476.1:p.Arg122=
|
|
NM_001030018.1:c.364A>C
|
NP_001025189.1:p.Arg122=
|
|
NM_000485.3:c.364A>C
MANE Select
|
NP_000476.1:p.Arg122=
|
|
NM_001030018.2:c.364A>C
|
NP_001025189.1:p.Arg122=
|
|