ENST00000378364.8:c.389T=
MANE Select
|
ENSP00000367615.3:p.Leu130=
|
|
ENST00000378364.7:c.389T=
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ENSP00000367615.3:p.Leu130=
|
|
ENST00000426324.6:c.389T=
|
ENSP00000397007.2:p.Leu130=
|
|
ENST00000562464.1:n.399T=
|
|
|
ENST00000563655.5:c.308T=
|
ENSP00000456012.1:p.Leu103=
|
|
ENST00000567057.5:n.188T=
|
|
|
ENST00000567391.5:c.*63T=
|
ENSP00000457964.1:n.*63T=
|
|
ENST00000567713.5:c.321+342T=
|
ENSP00000455749.1:n.321+342T=
|
|
ENST00000568319.5:c.*63T=
|
ENSP00000456905.1:n.*63T=
|
|
ENST00000568575.1:n.318T=
|
|
|
ENST00000569616.1:c.387T=
|
|
|
NM_000485.2:c.389T=
|
NP_000476.1:p.Leu130=
|
|
NM_001030018.1:c.389T=
|
NP_001025189.1:p.Leu130=
|
|
NM_000485.3:c.389T=
MANE Select
|
NP_000476.1:p.Leu130=
|
|
NM_001030018.2:c.389T=
|
NP_001025189.1:p.Leu130=
|
|