ENST00000373344.11:c.4375G>T
MANE Select
|
ENSP00000362441.4:p.Glu1459Ter
|
|
ENST00000373344.9:c.4375G>T
|
ENSP00000362441.4:p.Glu1459Ter
|
|
ENST00000395603.7:c.4261G>T
|
ENSP00000378967.3:p.Glu1421Ter
|
|
ENST00000480283.5:c.*4003G>T
|
ENSP00000480196.1:n.*4003G>T
|
|
NM_000489.4:c.4375G>T
|
NP_000480.3:p.Glu1459Ter
|
|
NM_138270.3:c.4261G>T
|
NP_612114.2:p.Glu1421Ter
|
|
XM_005262153.3:c.4372G>T
|
XP_005262210.2:p.Glu1458Ter
|
|
XM_005262154.3:c.4288G>T
|
XP_005262211.2:p.Glu1430Ter
|
|
XM_005262155.3:c.4258G>T
|
XP_005262212.2:p.Glu1420Ter
|
|
XM_005262156.3:c.4210G>T
|
XP_005262213.2:p.Glu1404Ter
|
|
XM_005262157.3:c.4171G>T
|
XP_005262214.2:p.Glu1391Ter
|
|
XM_006724666.2:c.4258G>T
|
XP_006724729.1:p.Glu1420Ter
|
|
XM_006724667.2:c.4096G>T
|
XP_006724730.1:p.Glu1366Ter
|
|
XM_006724668.2:c.4375G>T
|
XP_006724731.1:p.Glu1459Ter
|
|
XR_938400.1:n.4643G>T
|
|
|
NM_000489.5:c.4375G>T
|
NP_000480.3:p.Glu1459Ter
|
|
XM_005262153.5:c.4372G>T
|
XP_005262210.2:p.Glu1458Ter
|
|
XM_005262154.5:c.4288G>T
|
XP_005262211.2:p.Glu1430Ter
|
|
XM_005262155.4:c.4258G>T
|
XP_005262212.2:p.Glu1420Ter
|
|
XM_005262156.4:c.4210G>T
|
XP_005262213.2:p.Glu1404Ter
|
|
XM_005262157.5:c.4171G>T
|
XP_005262214.2:p.Glu1391Ter
|
|
XM_006724666.4:c.4258G>T
|
XP_006724729.1:p.Glu1420Ter
|
|
XM_006724667.3:c.4096G>T
|
XP_006724730.1:p.Glu1366Ter
|
|
XM_006724668.3:c.4375G>T
|
XP_006724731.1:p.Glu1459Ter
|
|
XM_017029601.2:c.4285G>T
|
XP_016885090.1:p.Glu1429Ter
|
|
XM_017029602.1:c.4255G>T
|
XP_016885091.1:p.Glu1419Ter
|
|
XM_017029603.1:c.4207G>T
|
XP_016885092.1:p.Glu1403Ter
|
|
XM_017029604.2:c.4174G>T
|
XP_016885093.1:p.Glu1392Ter
|
|
XM_017029605.1:c.4171G>T
|
XP_016885094.1:p.Glu1391Ter
|
|
XM_017029606.2:c.4144G>T
|
XP_016885095.1:p.Glu1382Ter
|
|
XM_017029607.2:c.4141G>T
|
XP_016885096.1:p.Glu1381Ter
|
|
XM_017029608.2:c.4093G>T
|
XP_016885097.1:p.Glu1365Ter
|
|
XM_017029609.1:c.4057G>T
|
XP_016885098.1:p.Glu1353Ter
|
|
XM_017029610.1:c.4054G>T
|
XP_016885099.1:p.Glu1352Ter
|
|
XM_017029611.1:c.4009G>T
|
XP_016885100.1:p.Glu1337Ter
|
|
XR_001755700.2:n.4600G>T
|
|
|
NM_138270.4:c.4261G>T
|
NP_612114.2:p.Glu1421Ter
|
|
NM_000489.6:c.4375G>T
MANE Select
|
NP_000480.3:p.Glu1459Ter
|
|
NM_138270.5:c.4261G>T
|
NP_612114.2:p.Glu1421Ter
|
|