|
NM_000051.4:c.8541G>T
(ATM)
MANE Select
|
NP_000042.3:p.Glu2847Asp
|
|
ENST00000675843.1:c.8541G>T
(ATM)
MANE Select
|
ENSP00000501606.1:p.Glu2847Asp
|
|
NM_000051.3:c.8541G>T , LRG_135t1:c.8541G>T
(ATM)
|
NP_000042.3:p.Glu2847Asp
|
|
NM_001330368.1:c.641-36794C>A
(C11orf65)
|
NP_001317297.1:n.641-36794C>A
|
|
NM_001330368.2:c.641-36794C>A
(C11orf65)
|
NP_001317297.1:n.641-36794C>A
|
|
NM_001351110.1:c.695-10573C>A
(C11orf65)
|
NP_001338039.1:n.695-10573C>A
|
|
NM_001351110.2:c.695-10573C>A
(C11orf65)
|
NP_001338039.1:n.695-10573C>A
|
|
NM_001351834.1:c.8541G>T
(ATM)
|
NP_001338763.1:p.Glu2847Asp
|
|
NM_001351834.2:c.8541G>T
(ATM)
|
NP_001338763.1:p.Glu2847Asp
|
|
NR_147053.2:n.2301+9050C>A
(C11orf65)
|
|
|
NR_147053.3:n.2299+9050C>A
(C11orf65)
|
|
|
ENST00000278616.8:c.8541G>T
(ATM)
|
ENSP00000278616.4:p.Glu2847Asp
|
|
ENST00000278616.9:c.8541G>T
(ATM)
|
ENSP00000278616.4:p.Glu2847Asp
|
|
ENST00000452508.6:c.8541G>T
(ATM)
|
ENSP00000388058.2:p.Glu2847Asp
|
|
ENST00000452508.7:c.8541G>T
(ATM)
|
ENSP00000388058.2:p.Glu2847Asp
|
|
ENST00000524755.5:c.227-10573C>A
(C11orf65)
|
|
|
ENST00000524792.5:n.4756G>T
(ATM)
|
|
|
ENST00000525729.5:c.641-36794C>A
(C11orf65)
|
ENSP00000433395.1:n.641-36794C>A
|
|
ENST00000526725.1:n.272-5501C>A
(C11orf65)
|
|
|
ENST00000527531.5:c.*1196+9050C>A
(C11orf65)
|
ENSP00000431706.1:n.*1196+9050C>A
|
|
ENST00000527805.6:c.*3605G>T
(ATM)
|
ENSP00000435747.2:n.*3605G>T
|
|
ENST00000615746.4:c.*1196+9050C>A
(C11orf65)
|
ENSP00000483537.1:n.*1196+9050C>A
|
|
ENST00000638786.2:n.1239G>T
(ATM)
|
|
|
ENST00000675595.1:c.*3676G>T
(ATM)
|
ENSP00000502563.1:n.*3676G>T
|
|
ENST00000682286.1:n.3298G>T
(ATM)
|
|
|
ENST00000682302.1:n.2959G>T
(ATM)
|
|
|
ENST00000683174.1:n.10025G>T
(ATM)
|
|
|
ENST00000683524.1:n.3765G>T
(ATM)
|
|
|
ENST00000684152.1:n.3957G>T
(ATM)
|
|
|
ENST00000684180.1:n.1015G>T
(ATM)
|
|
|
ENST00000684447.1:n.5034G>T
(ATM)
|
|
|
ENST00000713593.1:c.*8012G>T
(ATM)
|
ENSP00000518889.1:n.*8012G>T
|
|
XM_005271414.3:c.788-10573C>A
(C11orf65)
|
XP_005271471.1:n.788-10573C>A
|
|
XM_005271414.4:c.788-10573C>A
(C11orf65)
|
XP_005271471.1:n.788-10573C>A
|
|
XM_005271415.3:c.732-10573C>A
(C11orf65)
|
XP_005271472.1:n.732-10573C>A
|
|
XM_005271415.4:c.732-10573C>A
(C11orf65)
|
XP_005271472.1:n.732-10573C>A
|
|
XM_005271561.3:c.8541G>T
(ATM)
|
XP_005271618.2:p.Glu2847Asp
|
|
XM_005271562.3:c.8541G>T
(ATM)
|
XP_005271619.2:p.Glu2847Asp
|
|
XM_005271562.5:c.8541G>T
(ATM)
|
XP_005271619.2:p.Glu2847Asp
|
|
XM_006718843.2:c.8541G>T
(ATM)
|
XP_006718906.1:p.Glu2847Asp
|
|
XM_006718843.4:c.8541G>T
(ATM)
|
XP_006718906.1:p.Glu2847Asp
|
|
XM_006718845.1:c.4497G>T
(ATM)
|
XP_006718908.1:p.Glu1499Asp
|
|
XM_006718845.2:c.4497G>T
(ATM)
|
XP_006718908.1:p.Glu1499Asp
|
|
XM_011542640.1:c.788-5501C>A
(C11orf65)
|
XP_011540942.1:n.788-5501C>A
|
|
XM_011542640.2:c.788-5501C>A
(C11orf65)
|
XP_011540942.1:n.788-5501C>A
|
|
XM_011542643.1:c.732-5501C>A
(C11orf65)
|
XP_011540945.1:n.732-5501C>A
|
|
XM_011542643.2:c.732-5501C>A
(C11orf65)
|
XP_011540945.1:n.732-5501C>A
|
|
XM_011542840.1:c.8541G>T
(ATM)
|
XP_011541142.1:p.Glu2847Asp
|
|
XM_011542840.3:c.8541G>T
(ATM)
|
XP_011541142.1:p.Glu2847Asp
|
|
XM_011542841.1:c.8541G>T
(ATM)
|
XP_011541143.1:p.Glu2847Asp
|
|
XM_011542842.1:c.8376G>T
(ATM)
|
XP_011541144.1:p.Glu2792Asp
|
|
XM_011542842.3:c.8376G>T
(ATM)
|
XP_011541144.1:p.Glu2792Asp
|
|
XM_011542843.1:c.8541G>T
(ATM)
|
XP_011541145.1:p.Glu2847Asp
|
|
XM_011542843.2:c.8541G>T
(ATM)
|
XP_011541145.1:p.Glu2847Asp
|
|
XM_011542844.1:c.7497G>T
(ATM)
|
XP_011541146.1:p.Glu2499Asp
|
|
XM_011542844.3:c.7497G>T
(ATM)
|
XP_011541146.1:p.Glu2499Asp
|
|
XM_011542845.1:c.7233G>T
(ATM)
|
XP_011541147.1:p.Glu2411Asp
|
|
XM_011542845.2:c.7233G>T
(ATM)
|
XP_011541147.1:p.Glu2411Asp
|
|
XM_011542847.1:c.3612G>T
(ATM)
|
XP_011541149.1:p.Glu1204Asp
|
|
XM_017017247.1:c.904-5501C>A
(C11orf65)
|
XP_016872736.1:n.904-5501C>A
|
|
XM_017017789.2:c.8541G>T
(ATM)
|
XP_016873278.1:p.Glu2847Asp
|
|
XM_017017790.2:c.8541G>T
(ATM)
|
XP_016873279.1:p.Glu2847Asp
|
