ENST00000378364.8:c.383A>T
MANE Select
|
ENSP00000367615.3:p.Asp128Val
|
|
ENST00000378364.7:c.383A>T
|
ENSP00000367615.3:p.Asp128Val
|
|
ENST00000426324.6:c.383A>T
|
ENSP00000397007.2:p.Asp128Val
|
|
ENST00000562464.1:n.393A>T
|
|
|
ENST00000563655.5:c.302A>T
|
ENSP00000456012.1:p.Asp101Val
|
|
ENST00000567057.5:n.182A>T
|
|
|
ENST00000567391.5:c.*57A>T
|
ENSP00000457964.1:n.*57A>T
|
|
ENST00000567713.5:c.321+336A>T
|
ENSP00000455749.1:n.321+336A>T
|
|
ENST00000568319.5:c.*57A>T
|
ENSP00000456905.1:n.*57A>T
|
|
ENST00000568575.1:n.312A>T
|
|
|
ENST00000569616.1:c.381A>T
|
|
|
NM_000485.2:c.383A>T
|
NP_000476.1:p.Asp128Val
|
|
NM_001030018.1:c.383A>T
|
NP_001025189.1:p.Asp128Val
|
|
NM_000485.3:c.383A>T
MANE Select
|
NP_000476.1:p.Asp128Val
|
|
NM_001030018.2:c.383A>T
|
NP_001025189.1:p.Asp128Val
|
|