NM_138477.4:c.1705G>C
MANE Select
|
NP_612486.2:p.Gly569Arg
|
ENST00000356231.4:c.1705G>C
MANE Select
|
ENSP00000348564.3:p.Gly569Arg
|
NM_138477.2:c.1705G>C
|
NP_612486.2:p.Gly569Arg
|
ENST00000356231.3:c.1705G>C
|
ENSP00000348564.3:p.Gly569Arg
|
ENST00000643434.1:c.*883G>C
|
ENSP00000494699.1:n.*883G>C
|
XM_005254176.3:c.1708G>C
|
XP_005254233.1:p.Gly570Arg
|
XM_005254176.5:c.1708G>C
|
XP_005254233.1:p.Gly570Arg
|
XM_011521270.1:c.1732G>C
|
XP_011519572.1:p.Gly578Arg
|
XM_011521270.2:c.1732G>C
|
XP_011519572.1:p.Gly578Arg
|
XM_011521271.1:c.1729G>C
|
XP_011519573.1:p.Gly577Arg
|
XM_011521271.2:c.1729G>C
|
XP_011519573.1:p.Gly577Arg
|
XM_011521272.1:c.1732G>C
|
XP_011519574.1:p.Gly578Arg
|
XM_011521273.1:c.1732G>C
|
XP_011519575.1:p.Gly578Arg
|
XM_011521274.1:c.697G>C
|
XP_011519576.1:p.Gly233Arg
|
XM_011521274.2:c.697G>C
|
XP_011519576.1:p.Gly233Arg
|
XM_011521275.1:c.949G>C
|
XP_011519577.1:p.Gly317Arg
|
XR_001751104.1:n.1762G>C
|
|
XR_001751105.1:n.1762G>C
|
|
XR_931757.1:n.1743G>C
|
|
XR_931757.2:n.1763G>C
|
|