ENST00000691183.1:c.*168T=
|
ENSP00000509954.1:n.*168T=
|
|
ENST00000378842.8:c.580T=
MANE Select
|
ENSP00000368119.4:p.Phe194=
|
|
ENST00000378842.7:c.580T=
|
ENSP00000368119.3:p.Phe194=
|
|
ENST00000450095.6:c.253T=
|
ENSP00000401956.2:p.Phe85=
|
|
ENST00000472111.5:n.836T=
|
|
|
ENST00000473506.6:c.*168T=
|
ENSP00000432839.2:n.*168T=
|
|
ENST00000473529.5:n.739T=
|
|
|
ENST00000485531.1:n.1174T=
|
|
|
ENST00000487381.5:n.965T=
|
|
|
ENST00000489643.6:n.355T=
|
|
|
ENST00000554085.5:c.*324T=
|
ENSP00000450419.1:n.*324T=
|
|
ENST00000554139.5:n.826T=
|
|
|
ENST00000554550.5:c.*200T=
|
ENSP00000451435.1:n.*200T=
|
|
ENST00000554638.5:n.1052T=
|
|
|
ENST00000554897.5:c.*267T=
|
ENSP00000450942.1:n.*267T=
|
|
ENST00000554944.5:n.929T=
|
|
|
ENST00000555020.5:n.736T=
|
|
|
ENST00000555086.5:n.584T=
|
|
|
ENST00000555214.5:n.401T=
|
|
|
ENST00000556244.1:c.567T=
|
|
|
ENST00000556278.1:c.325T=
|
ENSP00000451792.1:p.Phe109=
|
|
ENST00000556494.5:n.701T=
|
|
|
ENST00000557706.5:n.1142T=
|
|
|
NM_000155.3:c.580T=
|
NP_000146.2:p.Phe194=
|
|
NM_001258332.1:c.253T=
|
NP_001245261.1:p.Phe85=
|
|
NM_000155.4:c.580T=
MANE Select
|
NP_000146.2:p.Phe194=
|
|
NM_001258332.2:c.253T=
|
NP_001245261.1:p.Phe85=
|
|