|
ENST00000356231.4:c.2671C>T
MANE Select
|
ENSP00000348564.3:p.Arg891Cys
|
|
|
ENST00000643434.1:c.*1849C>T
|
ENSP00000494699.1:n.*1849C>T
|
|
|
ENST00000356231.3:c.2671C>T
|
ENSP00000348564.3:p.Arg891Cys
|
|
|
ENST00000562465.5:c.664C>T
|
ENSP00000454246.1:p.Arg222Cys
|
|
|
NM_138477.2:c.2671C>T
|
NP_612486.2:p.Arg891Cys
|
|
|
XM_005254176.3:c.2674C>T
|
XP_005254233.1:p.Arg892Cys
|
|
|
XM_011521270.1:c.2698C>T
|
XP_011519572.1:p.Arg900Cys
|
|
|
XM_011521271.1:c.2695C>T
|
XP_011519573.1:p.Arg899Cys
|
|
|
XM_011521272.1:c.2698C>T
|
XP_011519574.1:p.Arg900Cys
|
|
|
XM_011521273.1:c.2698C>T
|
XP_011519575.1:p.Arg900Cys
|
|
|
XM_011521274.1:c.1663C>T
|
XP_011519576.1:p.Arg555Cys
|
|
|
XM_011521275.1:c.1915C>T
|
XP_011519577.1:p.Arg639Cys
|
|
|
NM_138477.4:c.2671C>T
MANE Select
|
NP_612486.2:p.Arg891Cys
|
|
|
XM_005254176.5:c.2674C>T
|
XP_005254233.1:p.Arg892Cys
|
|
|
XM_011521270.2:c.2698C>T
|
XP_011519572.1:p.Arg900Cys
|
|
|
XM_011521271.2:c.2695C>T
|
XP_011519573.1:p.Arg899Cys
|
|
|
XM_011521274.2:c.1663C>T
|
XP_011519576.1:p.Arg555Cys
|
|
|
XR_001751104.1:n.2728C>T
|
|
|
|
XR_001751105.1:n.2728C>T
|
|
|
