ENST00000691183.1:c.*373G=
|
ENSP00000509954.1:n.*373G=
|
|
ENST00000378842.8:c.785G=
MANE Select
|
ENSP00000368119.4:p.Arg262=
|
|
ENST00000378842.7:c.785G=
|
ENSP00000368119.3:p.Arg262=
|
|
ENST00000450095.6:c.458G=
|
ENSP00000401956.2:p.Arg153=
|
|
ENST00000473506.6:c.*373G=
|
ENSP00000432839.2:n.*373G=
|
|
ENST00000489643.6:n.865G=
|
|
|
ENST00000554085.5:c.*529G=
|
ENSP00000450419.1:n.*529G=
|
|
ENST00000554550.5:c.*405G=
|
ENSP00000451435.1:n.*405G=
|
|
ENST00000554638.5:n.1257G=
|
|
|
ENST00000555020.5:n.1246G=
|
|
|
ENST00000555086.5:n.789G=
|
|
|
ENST00000555754.1:n.130G=
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|
|
ENST00000556244.1:c.772G=
|
|
|
ENST00000556278.1:c.432+403G=
|
ENSP00000451792.1:n.432+403G=
|
|
ENST00000557706.5:n.1347G=
|
|
|
NM_000155.3:c.785G=
|
NP_000146.2:p.Arg262=
|
|
NM_001258332.1:c.458G=
|
NP_001245261.1:p.Arg153=
|
|
NM_000155.4:c.785G=
MANE Select
|
NP_000146.2:p.Arg262=
|
|
NM_001258332.2:c.458G=
|
NP_001245261.1:p.Arg153=
|
|