ENST00000373344.11:c.4433A>T
MANE Select
|
ENSP00000362441.4:p.Lys1478Met
|
|
ENST00000373344.9:c.4433A>T
|
ENSP00000362441.4:p.Lys1478Met
|
|
ENST00000395603.7:c.4319A>T
|
ENSP00000378967.3:p.Lys1440Met
|
|
ENST00000480283.5:c.*4061A>T
|
ENSP00000480196.1:n.*4061A>T
|
|
ENST00000623242.3:c.39A>T
|
|
|
NM_000489.4:c.4433A>T
|
NP_000480.3:p.Lys1478Met
|
|
NM_138270.3:c.4319A>T
|
NP_612114.2:p.Lys1440Met
|
|
XM_005262153.3:c.4430A>T
|
XP_005262210.2:p.Lys1477Met
|
|
XM_005262154.3:c.4346A>T
|
XP_005262211.2:p.Lys1449Met
|
|
XM_005262155.3:c.4316A>T
|
XP_005262212.2:p.Lys1439Met
|
|
XM_005262156.3:c.4268A>T
|
XP_005262213.2:p.Lys1423Met
|
|
XM_005262157.3:c.4229A>T
|
XP_005262214.2:p.Lys1410Met
|
|
XM_006724666.2:c.4316A>T
|
XP_006724729.1:p.Lys1439Met
|
|
XM_006724667.2:c.4154A>T
|
XP_006724730.1:p.Lys1385Met
|
|
XM_006724668.2:c.4433A>T
|
XP_006724731.1:p.Lys1478Met
|
|
XR_938400.1:n.4701A>T
|
|
|
NM_000489.5:c.4433A>T
|
NP_000480.3:p.Lys1478Met
|
|
XM_005262153.5:c.4430A>T
|
XP_005262210.2:p.Lys1477Met
|
|
XM_005262154.5:c.4346A>T
|
XP_005262211.2:p.Lys1449Met
|
|
XM_005262155.4:c.4316A>T
|
XP_005262212.2:p.Lys1439Met
|
|
XM_005262156.4:c.4268A>T
|
XP_005262213.2:p.Lys1423Met
|
|
XM_005262157.5:c.4229A>T
|
XP_005262214.2:p.Lys1410Met
|
|
XM_006724666.4:c.4316A>T
|
XP_006724729.1:p.Lys1439Met
|
|
XM_006724667.3:c.4154A>T
|
XP_006724730.1:p.Lys1385Met
|
|
XM_006724668.3:c.4433A>T
|
XP_006724731.1:p.Lys1478Met
|
|
XM_017029601.2:c.4343A>T
|
XP_016885090.1:p.Lys1448Met
|
|
XM_017029602.1:c.4313A>T
|
XP_016885091.1:p.Lys1438Met
|
|
XM_017029603.1:c.4265A>T
|
XP_016885092.1:p.Lys1422Met
|
|
XM_017029604.2:c.4232A>T
|
XP_016885093.1:p.Lys1411Met
|
|
XM_017029605.1:c.4229A>T
|
XP_016885094.1:p.Lys1410Met
|
|
XM_017029606.2:c.4202A>T
|
XP_016885095.1:p.Lys1401Met
|
|
XM_017029607.2:c.4199A>T
|
XP_016885096.1:p.Lys1400Met
|
|
XM_017029608.2:c.4151A>T
|
XP_016885097.1:p.Lys1384Met
|
|
XM_017029609.1:c.4115A>T
|
XP_016885098.1:p.Lys1372Met
|
|
XM_017029610.1:c.4112A>T
|
XP_016885099.1:p.Lys1371Met
|
|
XM_017029611.1:c.4067A>T
|
XP_016885100.1:p.Lys1356Met
|
|
XR_001755700.2:n.4658A>T
|
|
|
NM_138270.4:c.4319A>T
|
NP_612114.2:p.Lys1440Met
|
|
NM_000489.6:c.4433A>T
MANE Select
|
NP_000480.3:p.Lys1478Met
|
|
NM_138270.5:c.4319A>T
|
NP_612114.2:p.Lys1440Met
|
|