ENST00000373344.11:c.4492A>C
MANE Select
|
ENSP00000362441.4:p.Lys1498Gln
|
|
ENST00000373344.9:c.4492A>C
|
ENSP00000362441.4:p.Lys1498Gln
|
|
ENST00000395603.7:c.4378A>C
|
ENSP00000378967.3:p.Lys1460Gln
|
|
ENST00000480283.5:c.*4120A>C
|
ENSP00000480196.1:n.*4120A>C
|
|
ENST00000623242.3:c.98A>C
|
|
|
NM_000489.4:c.4492A>C
|
NP_000480.3:p.Lys1498Gln
|
|
NM_138270.3:c.4378A>C
|
NP_612114.2:p.Lys1460Gln
|
|
XM_005262153.3:c.4489A>C
|
XP_005262210.2:p.Lys1497Gln
|
|
XM_005262154.3:c.4405A>C
|
XP_005262211.2:p.Lys1469Gln
|
|
XM_005262155.3:c.4375A>C
|
XP_005262212.2:p.Lys1459Gln
|
|
XM_005262156.3:c.4327A>C
|
XP_005262213.2:p.Lys1443Gln
|
|
XM_005262157.3:c.4288A>C
|
XP_005262214.2:p.Lys1430Gln
|
|
XM_006724666.2:c.4375A>C
|
XP_006724729.1:p.Lys1459Gln
|
|
XM_006724667.2:c.4213A>C
|
XP_006724730.1:p.Lys1405Gln
|
|
XM_006724668.2:c.4492A>C
|
XP_006724731.1:p.Lys1498Gln
|
|
XR_938400.1:n.4760A>C
|
|
|
NM_000489.5:c.4492A>C
|
NP_000480.3:p.Lys1498Gln
|
|
XM_005262153.5:c.4489A>C
|
XP_005262210.2:p.Lys1497Gln
|
|
XM_005262154.5:c.4405A>C
|
XP_005262211.2:p.Lys1469Gln
|
|
XM_005262155.4:c.4375A>C
|
XP_005262212.2:p.Lys1459Gln
|
|
XM_005262156.4:c.4327A>C
|
XP_005262213.2:p.Lys1443Gln
|
|
XM_005262157.5:c.4288A>C
|
XP_005262214.2:p.Lys1430Gln
|
|
XM_006724666.4:c.4375A>C
|
XP_006724729.1:p.Lys1459Gln
|
|
XM_006724667.3:c.4213A>C
|
XP_006724730.1:p.Lys1405Gln
|
|
XM_006724668.3:c.4492A>C
|
XP_006724731.1:p.Lys1498Gln
|
|
XM_017029601.2:c.4402A>C
|
XP_016885090.1:p.Lys1468Gln
|
|
XM_017029602.1:c.4372A>C
|
XP_016885091.1:p.Lys1458Gln
|
|
XM_017029603.1:c.4324A>C
|
XP_016885092.1:p.Lys1442Gln
|
|
XM_017029604.2:c.4291A>C
|
XP_016885093.1:p.Lys1431Gln
|
|
XM_017029605.1:c.4288A>C
|
XP_016885094.1:p.Lys1430Gln
|
|
XM_017029606.2:c.4261A>C
|
XP_016885095.1:p.Lys1421Gln
|
|
XM_017029607.2:c.4258A>C
|
XP_016885096.1:p.Lys1420Gln
|
|
XM_017029608.2:c.4210A>C
|
XP_016885097.1:p.Lys1404Gln
|
|
XM_017029609.1:c.4174A>C
|
XP_016885098.1:p.Lys1392Gln
|
|
XM_017029610.1:c.4171A>C
|
XP_016885099.1:p.Lys1391Gln
|
|
XM_017029611.1:c.4126A>C
|
XP_016885100.1:p.Lys1376Gln
|
|
XR_001755700.2:n.4717A>C
|
|
|
NM_138270.4:c.4378A>C
|
NP_612114.2:p.Lys1460Gln
|
|
NM_000489.6:c.4492A>C
MANE Select
|
NP_000480.3:p.Lys1498Gln
|
|
NM_138270.5:c.4378A>C
|
NP_612114.2:p.Lys1460Gln
|
|