ENST00000373344.11:c.4443G>C
MANE Select
|
ENSP00000362441.4:p.Arg1481=
|
|
ENST00000373344.9:c.4443G>C
|
ENSP00000362441.4:p.Arg1481=
|
|
ENST00000395603.7:c.4329G>C
|
ENSP00000378967.3:p.Arg1443=
|
|
ENST00000480283.5:c.*4071G>C
|
ENSP00000480196.1:n.*4071G>C
|
|
ENST00000623242.3:c.49G>C
|
|
|
NM_000489.4:c.4443G>C
|
NP_000480.3:p.Arg1481=
|
|
NM_138270.3:c.4329G>C
|
NP_612114.2:p.Arg1443=
|
|
XM_005262153.3:c.4440G>C
|
XP_005262210.2:p.Arg1480=
|
|
XM_005262154.3:c.4356G>C
|
XP_005262211.2:p.Arg1452=
|
|
XM_005262155.3:c.4326G>C
|
XP_005262212.2:p.Arg1442=
|
|
XM_005262156.3:c.4278G>C
|
XP_005262213.2:p.Arg1426=
|
|
XM_005262157.3:c.4239G>C
|
XP_005262214.2:p.Arg1413=
|
|
XM_006724666.2:c.4326G>C
|
XP_006724729.1:p.Arg1442=
|
|
XM_006724667.2:c.4164G>C
|
XP_006724730.1:p.Arg1388=
|
|
XM_006724668.2:c.4443G>C
|
XP_006724731.1:p.Arg1481=
|
|
XR_938400.1:n.4711G>C
|
|
|
NM_000489.5:c.4443G>C
|
NP_000480.3:p.Arg1481=
|
|
XM_005262153.5:c.4440G>C
|
XP_005262210.2:p.Arg1480=
|
|
XM_005262154.5:c.4356G>C
|
XP_005262211.2:p.Arg1452=
|
|
XM_005262155.4:c.4326G>C
|
XP_005262212.2:p.Arg1442=
|
|
XM_005262156.4:c.4278G>C
|
XP_005262213.2:p.Arg1426=
|
|
XM_005262157.5:c.4239G>C
|
XP_005262214.2:p.Arg1413=
|
|
XM_006724666.4:c.4326G>C
|
XP_006724729.1:p.Arg1442=
|
|
XM_006724667.3:c.4164G>C
|
XP_006724730.1:p.Arg1388=
|
|
XM_006724668.3:c.4443G>C
|
XP_006724731.1:p.Arg1481=
|
|
XM_017029601.2:c.4353G>C
|
XP_016885090.1:p.Arg1451=
|
|
XM_017029602.1:c.4323G>C
|
XP_016885091.1:p.Arg1441=
|
|
XM_017029603.1:c.4275G>C
|
XP_016885092.1:p.Arg1425=
|
|
XM_017029604.2:c.4242G>C
|
XP_016885093.1:p.Arg1414=
|
|
XM_017029605.1:c.4239G>C
|
XP_016885094.1:p.Arg1413=
|
|
XM_017029606.2:c.4212G>C
|
XP_016885095.1:p.Arg1404=
|
|
XM_017029607.2:c.4209G>C
|
XP_016885096.1:p.Arg1403=
|
|
XM_017029608.2:c.4161G>C
|
XP_016885097.1:p.Arg1387=
|
|
XM_017029609.1:c.4125G>C
|
XP_016885098.1:p.Arg1375=
|
|
XM_017029610.1:c.4122G>C
|
XP_016885099.1:p.Arg1374=
|
|
XM_017029611.1:c.4077G>C
|
XP_016885100.1:p.Arg1359=
|
|
XR_001755700.2:n.4668G>C
|
|
|
NM_138270.4:c.4329G>C
|
NP_612114.2:p.Arg1443=
|
|
NM_000489.6:c.4443G>C
MANE Select
|
NP_000480.3:p.Arg1481=
|
|
NM_138270.5:c.4329G>C
|
NP_612114.2:p.Arg1443=
|
|