ENST00000262367.10:c.4552G>A
MANE Select
|
ENSP00000262367.5:p.Asp1518Asn
|
|
ENST00000262367.9:c.4552G>A
|
ENSP00000262367.5:p.Asp1518Asn
|
|
ENST00000382070.7:c.4438G>A
|
ENSP00000371502.3:p.Asp1480Asn
|
|
ENST00000570939.2:c.3187G>A
|
ENSP00000461002.2:p.Asp1063Asn
|
|
ENST00000571763.5:n.342G>A
|
|
|
ENST00000574740.1:n.373G>A
|
|
|
ENST00000576720.1:n.3375G>A
|
|
|
NM_001079846.1:c.4438G>A
|
NP_001073315.1:p.Asp1480Asn
|
|
NM_004380.2:c.4552G>A
|
NP_004371.2:p.Asp1518Asn
|
|
XM_005255124.3:c.4507G>A
|
XP_005255181.1:p.Asp1503Asn
|
|
XM_005255125.3:c.4135G>A
|
XP_005255182.1:p.Asp1379Asn
|
|
XM_006720848.2:c.4291G>A
|
XP_006720911.1:p.Asp1431Asn
|
|
XM_011522380.1:c.4498G>A
|
XP_011520682.1:p.Asp1500Asn
|
|
XM_011522381.1:c.3799G>A
|
XP_011520683.1:p.Asp1267Asn
|
|
XM_005255124.4:c.4507G>A
|
XP_005255181.1:p.Asp1503Asn
|
|
XM_005255125.4:c.4135G>A
|
XP_005255182.1:p.Asp1379Asn
|
|
XM_006720848.3:c.4291G>A
|
XP_006720911.1:p.Asp1431Asn
|
|
XM_011522381.2:c.3799G>A
|
XP_011520683.1:p.Asp1267Asn
|
|
XM_017022944.1:c.4546G>A
|
XP_016878433.1:p.Asp1516Asn
|
|
NM_004380.3:c.4552G>A
MANE Select
|
NP_004371.2:p.Asp1518Asn
|
|