ENST00000373344.11:c.4326T>G
MANE Select
|
ENSP00000362441.4:p.Ser1442=
|
|
ENST00000373344.9:c.4326T>G
|
ENSP00000362441.4:p.Ser1442=
|
|
ENST00000395603.7:c.4212T>G
|
ENSP00000378967.3:p.Ser1404=
|
|
ENST00000480283.5:c.*3954T>G
|
ENSP00000480196.1:n.*3954T>G
|
|
NM_000489.4:c.4326T>G
|
NP_000480.3:p.Ser1442=
|
|
NM_138270.3:c.4212T>G
|
NP_612114.2:p.Ser1404=
|
|
XM_005262153.3:c.4323T>G
|
XP_005262210.2:p.Ser1441=
|
|
XM_005262154.3:c.4239T>G
|
XP_005262211.2:p.Ser1413=
|
|
XM_005262155.3:c.4209T>G
|
XP_005262212.2:p.Ser1403=
|
|
XM_005262156.3:c.4161T>G
|
XP_005262213.2:p.Ser1387=
|
|
XM_005262157.3:c.4122T>G
|
XP_005262214.2:p.Ser1374=
|
|
XM_006724666.2:c.4209T>G
|
XP_006724729.1:p.Ser1403=
|
|
XM_006724667.2:c.4047T>G
|
XP_006724730.1:p.Ser1349=
|
|
XM_006724668.2:c.4326T>G
|
XP_006724731.1:p.Ser1442=
|
|
XR_938400.1:n.4594T>G
|
|
|
NM_000489.5:c.4326T>G
|
NP_000480.3:p.Ser1442=
|
|
XM_005262153.5:c.4323T>G
|
XP_005262210.2:p.Ser1441=
|
|
XM_005262154.5:c.4239T>G
|
XP_005262211.2:p.Ser1413=
|
|
XM_005262155.4:c.4209T>G
|
XP_005262212.2:p.Ser1403=
|
|
XM_005262156.4:c.4161T>G
|
XP_005262213.2:p.Ser1387=
|
|
XM_005262157.5:c.4122T>G
|
XP_005262214.2:p.Ser1374=
|
|
XM_006724666.4:c.4209T>G
|
XP_006724729.1:p.Ser1403=
|
|
XM_006724667.3:c.4047T>G
|
XP_006724730.1:p.Ser1349=
|
|
XM_006724668.3:c.4326T>G
|
XP_006724731.1:p.Ser1442=
|
|
XM_017029601.2:c.4236T>G
|
XP_016885090.1:p.Ser1412=
|
|
XM_017029602.1:c.4206T>G
|
XP_016885091.1:p.Ser1402=
|
|
XM_017029603.1:c.4158T>G
|
XP_016885092.1:p.Ser1386=
|
|
XM_017029604.2:c.4125T>G
|
XP_016885093.1:p.Ser1375=
|
|
XM_017029605.1:c.4122T>G
|
XP_016885094.1:p.Ser1374=
|
|
XM_017029606.2:c.4095T>G
|
XP_016885095.1:p.Ser1365=
|
|
XM_017029607.2:c.4092T>G
|
XP_016885096.1:p.Ser1364=
|
|
XM_017029608.2:c.4044T>G
|
XP_016885097.1:p.Ser1348=
|
|
XM_017029609.1:c.4008T>G
|
XP_016885098.1:p.Ser1336=
|
|
XM_017029610.1:c.4005T>G
|
XP_016885099.1:p.Ser1335=
|
|
XM_017029611.1:c.3960T>G
|
XP_016885100.1:p.Ser1320=
|
|
XR_001755700.2:n.4551T>G
|
|
|
NM_138270.4:c.4212T>G
|
NP_612114.2:p.Ser1404=
|
|
NM_000489.6:c.4326T>G
MANE Select
|
NP_000480.3:p.Ser1442=
|
|
NM_138270.5:c.4212T>G
|
NP_612114.2:p.Ser1404=
|
|