NM_138477.4:c.3043C>A
MANE Select
|
NP_612486.2:p.Arg1015Ser
|
ENST00000356231.4:c.3043C>A
MANE Select
|
ENSP00000348564.3:p.Arg1015Ser
|
NM_138477.2:c.3043C>A
|
NP_612486.2:p.Arg1015Ser
|
ENST00000356231.3:c.3043C>A
|
ENSP00000348564.3:p.Arg1015Ser
|
ENST00000562465.5:c.1036C>A
|
ENSP00000454246.1:p.Arg346Ser
|
ENST00000643434.1:c.*2221C>A
|
ENSP00000494699.1:n.*2221C>A
|
XM_005254176.3:c.3046C>A
|
XP_005254233.1:p.Arg1016Ser
|
XM_005254176.5:c.3046C>A
|
XP_005254233.1:p.Arg1016Ser
|
XM_011521270.1:c.3070C>A
|
XP_011519572.1:p.Arg1024Ser
|
XM_011521270.2:c.3070C>A
|
XP_011519572.1:p.Arg1024Ser
|
XM_011521271.1:c.3067C>A
|
XP_011519573.1:p.Arg1023Ser
|
XM_011521271.2:c.3067C>A
|
XP_011519573.1:p.Arg1023Ser
|
XM_011521272.1:c.3070C>A
|
XP_011519574.1:p.Arg1024Ser
|
XM_011521273.1:c.3070C>A
|
XP_011519575.1:p.Arg1024Ser
|
XM_011521274.1:c.2035C>A
|
XP_011519576.1:p.Arg679Ser
|
XM_011521274.2:c.2035C>A
|
XP_011519576.1:p.Arg679Ser
|
XM_011521275.1:c.2287C>A
|
XP_011519577.1:p.Arg763Ser
|
XR_001751104.1:n.3100C>A
|
|
XR_001751105.1:n.3100C>A
|
|