ENST00000373344.11:c.4400A>G
MANE Select
|
ENSP00000362441.4:p.Asn1467Ser
|
|
ENST00000373344.9:c.4400A>G
|
ENSP00000362441.4:p.Asn1467Ser
|
|
ENST00000395603.7:c.4286A>G
|
ENSP00000378967.3:p.Asn1429Ser
|
|
ENST00000480283.5:c.*4028A>G
|
ENSP00000480196.1:n.*4028A>G
|
|
ENST00000623242.3:c.6A>G
|
|
|
NM_000489.4:c.4400A>G
|
NP_000480.3:p.Asn1467Ser
|
|
NM_138270.3:c.4286A>G
|
NP_612114.2:p.Asn1429Ser
|
|
XM_005262153.3:c.4397A>G
|
XP_005262210.2:p.Asn1466Ser
|
|
XM_005262154.3:c.4313A>G
|
XP_005262211.2:p.Asn1438Ser
|
|
XM_005262155.3:c.4283A>G
|
XP_005262212.2:p.Asn1428Ser
|
|
XM_005262156.3:c.4235A>G
|
XP_005262213.2:p.Asn1412Ser
|
|
XM_005262157.3:c.4196A>G
|
XP_005262214.2:p.Asn1399Ser
|
|
XM_006724666.2:c.4283A>G
|
XP_006724729.1:p.Asn1428Ser
|
|
XM_006724667.2:c.4121A>G
|
XP_006724730.1:p.Asn1374Ser
|
|
XM_006724668.2:c.4400A>G
|
XP_006724731.1:p.Asn1467Ser
|
|
XR_938400.1:n.4668A>G
|
|
|
NM_000489.5:c.4400A>G
|
NP_000480.3:p.Asn1467Ser
|
|
XM_005262153.5:c.4397A>G
|
XP_005262210.2:p.Asn1466Ser
|
|
XM_005262154.5:c.4313A>G
|
XP_005262211.2:p.Asn1438Ser
|
|
XM_005262155.4:c.4283A>G
|
XP_005262212.2:p.Asn1428Ser
|
|
XM_005262156.4:c.4235A>G
|
XP_005262213.2:p.Asn1412Ser
|
|
XM_005262157.5:c.4196A>G
|
XP_005262214.2:p.Asn1399Ser
|
|
XM_006724666.4:c.4283A>G
|
XP_006724729.1:p.Asn1428Ser
|
|
XM_006724667.3:c.4121A>G
|
XP_006724730.1:p.Asn1374Ser
|
|
XM_006724668.3:c.4400A>G
|
XP_006724731.1:p.Asn1467Ser
|
|
XM_017029601.2:c.4310A>G
|
XP_016885090.1:p.Asn1437Ser
|
|
XM_017029602.1:c.4280A>G
|
XP_016885091.1:p.Asn1427Ser
|
|
XM_017029603.1:c.4232A>G
|
XP_016885092.1:p.Asn1411Ser
|
|
XM_017029604.2:c.4199A>G
|
XP_016885093.1:p.Asn1400Ser
|
|
XM_017029605.1:c.4196A>G
|
XP_016885094.1:p.Asn1399Ser
|
|
XM_017029606.2:c.4169A>G
|
XP_016885095.1:p.Asn1390Ser
|
|
XM_017029607.2:c.4166A>G
|
XP_016885096.1:p.Asn1389Ser
|
|
XM_017029608.2:c.4118A>G
|
XP_016885097.1:p.Asn1373Ser
|
|
XM_017029609.1:c.4082A>G
|
XP_016885098.1:p.Asn1361Ser
|
|
XM_017029610.1:c.4079A>G
|
XP_016885099.1:p.Asn1360Ser
|
|
XM_017029611.1:c.4034A>G
|
XP_016885100.1:p.Asn1345Ser
|
|
XR_001755700.2:n.4625A>G
|
|
|
NM_138270.4:c.4286A>G
|
NP_612114.2:p.Asn1429Ser
|
|
NM_000489.6:c.4400A>G
MANE Select
|
NP_000480.3:p.Asn1467Ser
|
|
NM_138270.5:c.4286A>G
|
NP_612114.2:p.Asn1429Ser
|
|