ENST00000378364.8:c.537T>A
MANE Select
|
ENSP00000367615.3:p.Tyr179Ter
|
|
ENST00000378364.7:c.537T>A
|
ENSP00000367615.3:p.Tyr179Ter
|
|
ENST00000426324.6:c.403T>A
|
ENSP00000397007.2:p.Ter135Arg
|
|
ENST00000563655.5:c.456T>A
|
ENSP00000456012.1:p.Tyr152Ter
|
|
ENST00000567057.5:n.202T>A
|
|
|
ENST00000567391.5:c.*211T>A
|
ENSP00000457964.1:n.*211T>A
|
|
ENST00000567713.5:c.322-169T>A
|
ENSP00000455749.1:n.322-169T>A
|
|
ENST00000568319.5:c.*77T>A
|
ENSP00000456905.1:n.*77T>A
|
|
ENST00000568575.1:n.466T>A
|
|
|
ENST00000569616.1:c.602T>A
|
|
|
NM_000485.2:c.537T>A
|
NP_000476.1:p.Tyr179Ter
|
|
NM_001030018.1:c.403T>A
|
NP_001025189.1:p.Ter135Arg
|
|
NM_000485.3:c.537T>A
MANE Select
|
NP_000476.1:p.Tyr179Ter
|
|
NM_001030018.2:c.403T>A
|
NP_001025189.1:p.Ter135Arg
|
|