ENST00000378823.8:c.3844T>C
(RAD50)
MANE Select
|
ENSP00000368100.4:p.Tyr1282His
|
|
ENST00000638452.2:c.3547T>C
|
ENSP00000492349.2:p.Tyr1183His
|
|
ENST00000638504.1:n.3452T>C
|
|
|
ENST00000638568.2:c.3547T>C
|
ENSP00000491158.2:p.Tyr1183His
|
|
ENST00000639899.1:n.4363T>C
|
|
|
ENST00000640655.2:c.3547T>C
|
ENSP00000491596.2:p.Tyr1183His
|
|
ENST00000651249.1:c.680T>C
(RAD50)
|
|
|
ENST00000378823.7:c.3844T>C
(RAD50)
|
ENSP00000368100.4:p.Tyr1282His
|
|
ENST00000455677.1:c.388-736T>C
(RAD50)
|
|
|
ENST00000533482.5:c.*3470T>C
(RAD50)
|
ENSP00000431225.1:n.*3470T>C
|
|
NM_005732.3:c.3844T>C
(RAD50)
|
NP_005723.2:p.Tyr1282His
|
|
NR_132125.1:n.118A>G
(TH2LCRR)
|
|
|
NR_132126.1:n.175-4004A>G
(TH2LCRR)
|
|
|
NM_005732.4:c.3844T>C
(RAD50)
MANE Select
|
NP_005723.2:p.Tyr1282His
|
|