ENST00000578493.2:n.746C>A
|
|
|
ENST00000699291.1:c.538C>A
|
ENSP00000514272.1:p.His180Asn
|
|
ENST00000699292.1:n.453C>A
|
|
|
ENST00000225275.4:c.1413C>A
MANE Select
|
ENSP00000225275.3:p.Ala471=
|
|
ENST00000225275.3:c.1413C>A
|
ENSP00000225275.3:p.Ala471=
|
|
NM_000250.1:c.1413C>A , LRG_84t1:c.1413C>A
|
NP_000241.1:p.Ala471=
|
|
XM_011524821.1:c.1599C>A
|
XP_011523123.1:p.Ala533=
|
|
XM_011524822.1:c.1128C>A
|
XP_011523124.1:p.Ala376=
|
|
XM_011524823.1:c.1438C>A
|
XP_011523125.1:p.His480Asn
|
|
NM_000250.2:c.1413C>A
MANE Select
|
NP_000241.1:p.Ala471=
|
|