ENST00000378823.8:c.3454C>T
(RAD50)
MANE Select
|
ENSP00000368100.4:p.Arg1152Ter
|
|
ENST00000638452.2:c.3157C>T
|
ENSP00000492349.2:p.Arg1053Ter
|
|
ENST00000638504.1:n.3062C>T
|
|
|
ENST00000638568.2:c.3157C>T
|
ENSP00000491158.2:p.Arg1053Ter
|
|
ENST00000639899.1:n.3973C>T
|
|
|
ENST00000640655.2:c.3157C>T
|
ENSP00000491596.2:p.Arg1053Ter
|
|
ENST00000651249.1:c.290C>T
(RAD50)
|
|
|
ENST00000378823.7:c.3454C>T
(RAD50)
|
ENSP00000368100.4:p.Arg1152Ter
|
|
ENST00000455677.1:c.89C>T
(RAD50)
|
|
|
ENST00000533482.5:c.*3080C>T
(RAD50)
|
ENSP00000431225.1:n.*3080C>T
|
|
NM_005732.3:c.3454C>T
(RAD50)
|
NP_005723.2:p.Arg1152Ter
|
|
NR_132124.1:n.153+979G>A
(TH2LCRR)
|
|
|
NM_005732.4:c.3454C>T
(RAD50)
MANE Select
|
NP_005723.2:p.Arg1152Ter
|
|