ENST00000356231.4:c.1858C>G
MANE Select
|
ENSP00000348564.3:p.Gln620Glu
|
|
ENST00000643434.1:c.*1036C>G
|
ENSP00000494699.1:n.*1036C>G
|
|
ENST00000356231.3:c.1858C>G
|
ENSP00000348564.3:p.Gln620Glu
|
|
NM_138477.2:c.1858C>G
|
NP_612486.2:p.Gln620Glu
|
|
XM_005254176.3:c.1861C>G
|
XP_005254233.1:p.Gln621Glu
|
|
XM_011521270.1:c.1885C>G
|
XP_011519572.1:p.Gln629Glu
|
|
XM_011521271.1:c.1882C>G
|
XP_011519573.1:p.Gln628Glu
|
|
XM_011521272.1:c.1885C>G
|
XP_011519574.1:p.Gln629Glu
|
|
XM_011521273.1:c.1885C>G
|
XP_011519575.1:p.Gln629Glu
|
|
XM_011521274.1:c.850C>G
|
XP_011519576.1:p.Gln284Glu
|
|
XM_011521275.1:c.1102C>G
|
XP_011519577.1:p.Gln368Glu
|
|
XR_931757.1:n.1896C>G
|
|
|
NM_138477.4:c.1858C>G
MANE Select
|
NP_612486.2:p.Gln620Glu
|
|
XM_005254176.5:c.1861C>G
|
XP_005254233.1:p.Gln621Glu
|
|
XM_011521270.2:c.1885C>G
|
XP_011519572.1:p.Gln629Glu
|
|
XM_011521271.2:c.1882C>G
|
XP_011519573.1:p.Gln628Glu
|
|
XM_011521274.2:c.850C>G
|
XP_011519576.1:p.Gln284Glu
|
|
XR_001751104.1:n.1915C>G
|
|
|
XR_001751105.1:n.1915C>G
|
|
|
XR_931757.2:n.1916C>G
|
|
|