ENST00000373344.11:c.4446G>A
MANE Select
|
ENSP00000362441.4:p.Lys1482=
|
|
ENST00000373344.9:c.4446G>A
|
ENSP00000362441.4:p.Lys1482=
|
|
ENST00000395603.7:c.4332G>A
|
ENSP00000378967.3:p.Lys1444=
|
|
ENST00000480283.5:c.*4074G>A
|
ENSP00000480196.1:n.*4074G>A
|
|
ENST00000623242.3:c.52G>A
|
|
|
NM_000489.4:c.4446G>A
|
NP_000480.3:p.Lys1482=
|
|
NM_138270.3:c.4332G>A
|
NP_612114.2:p.Lys1444=
|
|
XM_005262153.3:c.4443G>A
|
XP_005262210.2:p.Lys1481=
|
|
XM_005262154.3:c.4359G>A
|
XP_005262211.2:p.Lys1453=
|
|
XM_005262155.3:c.4329G>A
|
XP_005262212.2:p.Lys1443=
|
|
XM_005262156.3:c.4281G>A
|
XP_005262213.2:p.Lys1427=
|
|
XM_005262157.3:c.4242G>A
|
XP_005262214.2:p.Lys1414=
|
|
XM_006724666.2:c.4329G>A
|
XP_006724729.1:p.Lys1443=
|
|
XM_006724667.2:c.4167G>A
|
XP_006724730.1:p.Lys1389=
|
|
XM_006724668.2:c.4446G>A
|
XP_006724731.1:p.Lys1482=
|
|
XR_938400.1:n.4714G>A
|
|
|
NM_000489.5:c.4446G>A
|
NP_000480.3:p.Lys1482=
|
|
XM_005262153.5:c.4443G>A
|
XP_005262210.2:p.Lys1481=
|
|
XM_005262154.5:c.4359G>A
|
XP_005262211.2:p.Lys1453=
|
|
XM_005262155.4:c.4329G>A
|
XP_005262212.2:p.Lys1443=
|
|
XM_005262156.4:c.4281G>A
|
XP_005262213.2:p.Lys1427=
|
|
XM_005262157.5:c.4242G>A
|
XP_005262214.2:p.Lys1414=
|
|
XM_006724666.4:c.4329G>A
|
XP_006724729.1:p.Lys1443=
|
|
XM_006724667.3:c.4167G>A
|
XP_006724730.1:p.Lys1389=
|
|
XM_006724668.3:c.4446G>A
|
XP_006724731.1:p.Lys1482=
|
|
XM_017029601.2:c.4356G>A
|
XP_016885090.1:p.Lys1452=
|
|
XM_017029602.1:c.4326G>A
|
XP_016885091.1:p.Lys1442=
|
|
XM_017029603.1:c.4278G>A
|
XP_016885092.1:p.Lys1426=
|
|
XM_017029604.2:c.4245G>A
|
XP_016885093.1:p.Lys1415=
|
|
XM_017029605.1:c.4242G>A
|
XP_016885094.1:p.Lys1414=
|
|
XM_017029606.2:c.4215G>A
|
XP_016885095.1:p.Lys1405=
|
|
XM_017029607.2:c.4212G>A
|
XP_016885096.1:p.Lys1404=
|
|
XM_017029608.2:c.4164G>A
|
XP_016885097.1:p.Lys1388=
|
|
XM_017029609.1:c.4128G>A
|
XP_016885098.1:p.Lys1376=
|
|
XM_017029610.1:c.4125G>A
|
XP_016885099.1:p.Lys1375=
|
|
XM_017029611.1:c.4080G>A
|
XP_016885100.1:p.Lys1360=
|
|
XR_001755700.2:n.4671G>A
|
|
|
NM_138270.4:c.4332G>A
|
NP_612114.2:p.Lys1444=
|
|
NM_000489.6:c.4446G>A
MANE Select
|
NP_000480.3:p.Lys1482=
|
|
NM_138270.5:c.4332G>A
|
NP_612114.2:p.Lys1444=
|
|