ENST00000691183.1:c.*228G=
|
ENSP00000509954.1:n.*228G=
|
|
ENST00000378842.8:c.640G=
MANE Select
|
ENSP00000368119.4:p.Gly214=
|
|
ENST00000378842.7:c.640G=
|
ENSP00000368119.3:p.Gly214=
|
|
ENST00000450095.6:c.313G=
|
ENSP00000401956.2:p.Gly105=
|
|
ENST00000472111.5:n.896G=
|
|
|
ENST00000473506.6:c.*228G=
|
ENSP00000432839.2:n.*228G=
|
|
ENST00000473529.5:n.799G=
|
|
|
ENST00000487381.5:n.1025G=
|
|
|
ENST00000489643.6:n.415G=
|
|
|
ENST00000554085.5:c.*384G=
|
ENSP00000450419.1:n.*384G=
|
|
ENST00000554550.5:c.*260G=
|
ENSP00000451435.1:n.*260G=
|
|
ENST00000554638.5:n.1112G=
|
|
|
ENST00000555020.5:n.796G=
|
|
|
ENST00000555086.5:n.644G=
|
|
|
ENST00000555214.5:n.461G=
|
|
|
ENST00000556244.1:c.627G=
|
|
|
ENST00000556278.1:c.385G=
|
ENSP00000451792.1:p.Gly129=
|
|
ENST00000556494.5:n.761G=
|
|
|
ENST00000557706.5:n.1202G=
|
|
|
NM_000155.3:c.640G=
|
NP_000146.2:p.Gly214=
|
|
NM_001258332.1:c.313G=
|
NP_001245261.1:p.Gly105=
|
|
NM_000155.4:c.640G=
MANE Select
|
NP_000146.2:p.Gly214=
|
|
NM_001258332.2:c.313G=
|
NP_001245261.1:p.Gly105=
|
|