ENST00000578493.2:n.802T>A
|
|
|
ENST00000699291.1:c.594T>A
|
ENSP00000514272.1:n.594T>A
|
|
ENST00000699292.1:n.509T>A
|
|
|
ENST00000225275.4:c.1469T>A
MANE Select
|
ENSP00000225275.3:p.Ile490Asn
|
|
ENST00000225275.3:c.1469T>A
|
ENSP00000225275.3:p.Ile490Asn
|
|
NM_000250.1:c.1469T>A , LRG_84t1:c.1469T>A
|
NP_000241.1:p.Ile490Asn
|
|
XM_011524821.1:c.1655T>A
|
XP_011523123.1:p.Ile552Asn
|
|
XM_011524822.1:c.1184T>A
|
XP_011523124.1:p.Ile395Asn
|
|
XM_011524823.1:c.*18T>A
|
XP_011523125.1:n.*18T>A
|
|
NM_000250.2:c.1469T>A
MANE Select
|
NP_000241.1:p.Ile490Asn
|
|