ENST00000378364.8:c.267G>T
MANE Select
|
ENSP00000367615.3:p.Arg89=
|
|
ENST00000378364.7:c.267G>T
|
ENSP00000367615.3:p.Arg89=
|
|
ENST00000426324.6:c.267G>T
|
ENSP00000397007.2:p.Arg89=
|
|
ENST00000562464.1:n.332-329G>T
|
|
|
ENST00000563655.5:c.241-329G>T
|
ENSP00000456012.1:n.241-329G>T
|
|
ENST00000567391.5:c.188-329G>T
|
ENSP00000457964.1:n.188-329G>T
|
|
ENST00000567713.5:c.267G>T
|
ENSP00000455749.1:p.Arg89=
|
|
ENST00000568319.5:c.188-329G>T
|
ENSP00000456905.1:n.188-329G>T
|
|
ENST00000569616.1:c.265G>T
|
|
|
NM_000485.2:c.267G>T
|
NP_000476.1:p.Arg89=
|
|
NM_001030018.1:c.267G>T
|
NP_001025189.1:p.Arg89=
|
|
NM_000485.3:c.267G>T
MANE Select
|
NP_000476.1:p.Arg89=
|
|
NM_001030018.2:c.267G>T
|
NP_001025189.1:p.Arg89=
|
|