ENST00000262367.10:c.4412T>A
MANE Select
|
ENSP00000262367.5:p.Ile1471Asn
|
|
ENST00000262367.9:c.4412T>A
|
ENSP00000262367.5:p.Ile1471Asn
|
|
ENST00000382070.7:c.4298T>A
|
ENSP00000371502.3:p.Ile1433Asn
|
|
ENST00000570939.2:c.3047T>A
|
ENSP00000461002.2:p.Ile1016Asn
|
|
ENST00000571763.5:n.202T>A
|
|
|
ENST00000574740.1:n.233T>A
|
|
|
ENST00000576720.1:n.3235T>A
|
|
|
NM_001079846.1:c.4298T>A
|
NP_001073315.1:p.Ile1433Asn
|
|
NM_004380.2:c.4412T>A
|
NP_004371.2:p.Ile1471Asn
|
|
XM_005255124.3:c.4367T>A
|
XP_005255181.1:p.Ile1456Asn
|
|
XM_005255125.3:c.3995T>A
|
XP_005255182.1:p.Ile1332Asn
|
|
XM_006720848.2:c.4151T>A
|
XP_006720911.1:p.Ile1384Asn
|
|
XM_011522380.1:c.4358T>A
|
XP_011520682.1:p.Ile1453Asn
|
|
XM_011522381.1:c.3659T>A
|
XP_011520683.1:p.Ile1220Asn
|
|
XM_005255124.4:c.4367T>A
|
XP_005255181.1:p.Ile1456Asn
|
|
XM_005255125.4:c.3995T>A
|
XP_005255182.1:p.Ile1332Asn
|
|
XM_006720848.3:c.4151T>A
|
XP_006720911.1:p.Ile1384Asn
|
|
XM_011522381.2:c.3659T>A
|
XP_011520683.1:p.Ile1220Asn
|
|
XM_017022944.1:c.4406T>A
|
XP_016878433.1:p.Ile1469Asn
|
|
NM_004380.3:c.4412T>A
MANE Select
|
NP_004371.2:p.Ile1471Asn
|
|