NM_005732.4:c.3598C=
(RAD50)
MANE Select
|
NP_005723.2:p.Arg1200=
|
ENST00000378823.8:c.3598C=
(RAD50)
MANE Select
|
ENSP00000368100.4:p.Arg1200=
|
NM_005732.3:c.3598C=
(RAD50)
|
NP_005723.2:p.Arg1200=
|
NR_132124.1:n.108G=
(TH2LCRR)
|
|
NR_132125.1:n.252G=
(TH2LCRR)
|
|
NR_132126.1:n.237G=
(TH2LCRR)
|
|
ENST00000378823.7:c.3598C=
(RAD50)
|
ENSP00000368100.4:p.Arg1200=
|
ENST00000455677.1:c.233C=
(RAD50)
|
|
ENST00000533482.5:c.*3224C=
(RAD50)
|
ENSP00000431225.1:n.*3224C=
|
ENST00000638452.2:c.3301C=
|
ENSP00000492349.2:p.Arg1101=
|
ENST00000638504.1:n.3206C=
|
|
ENST00000638568.2:c.3301C=
|
ENSP00000491158.2:p.Arg1101=
|
ENST00000639899.1:n.4117C=
|
|
ENST00000640655.2:c.3301C=
|
ENSP00000491596.2:p.Arg1101=
|
ENST00000651249.1:c.434C=
(RAD50)
|
|
XR_427771.1:n.489G=
(TH2LCRR)
|
|