|
NM_000051.4:c.8914C>T
(ATM)
MANE Select
|
NP_000042.3:p.Gln2972Ter
|
|
ENST00000675843.1:c.8914C>T
(ATM)
MANE Select
|
ENSP00000501606.1:p.Gln2972Ter
|
|
NM_000051.3:c.8914C>T , LRG_135t1:c.8914C>T
(ATM)
|
NP_000042.3:p.Gln2972Ter
|
|
NM_001330368.1:c.640+20775G>A
(C11orf65)
|
NP_001317297.1:n.640+20775G>A
|
|
NM_001330368.2:c.640+20775G>A
(C11orf65)
|
NP_001317297.1:n.640+20775G>A
|
|
NM_001351110.1:c.694+20775G>A
(C11orf65)
|
NP_001338039.1:n.694+20775G>A
|
|
NM_001351110.2:c.694+20775G>A
(C11orf65)
|
NP_001338039.1:n.694+20775G>A
|
|
NM_001351834.1:c.8914C>T
(ATM)
|
NP_001338763.1:p.Gln2972Ter
|
|
NM_001351834.2:c.8914C>T
(ATM)
|
NP_001338763.1:p.Gln2972Ter
|
|
NR_147053.2:n.1107-9036G>A
(C11orf65)
|
|
|
NR_147053.3:n.1105-9036G>A
(C11orf65)
|
|
|
ENST00000278616.8:c.8914C>T
(ATM)
|
ENSP00000278616.4:p.Gln2972Ter
|
|
ENST00000278616.9:c.8914C>T
(ATM)
|
ENSP00000278616.4:p.Gln2972Ter
|
|
ENST00000452508.6:c.8914C>T
(ATM)
|
ENSP00000388058.2:p.Gln2972Ter
|
|
ENST00000452508.7:c.8914C>T
(ATM)
|
ENSP00000388058.2:p.Gln2972Ter
|
|
ENST00000524755.5:c.226+28063G>A
(C11orf65)
|
|
|
ENST00000524792.5:n.5129C>T
(ATM)
|
|
|
ENST00000525178.5:n.402C>T
(ATM)
|
|
|
ENST00000525729.5:c.640+20775G>A
(C11orf65)
|
ENSP00000433395.1:n.640+20775G>A
|
|
ENST00000526725.1:n.272-24781G>A
(C11orf65)
|
|
|
ENST00000527181.1:n.253C>T
(ATM)
|
|
|
ENST00000527531.5:c.*2-9036G>A
(C11orf65)
|
ENSP00000431706.1:n.*2-9036G>A
|
|
ENST00000527805.6:c.*3978C>T
(ATM)
|
ENSP00000435747.2:n.*3978C>T
|
|
ENST00000615746.4:c.*2-9036G>A
(C11orf65)
|
ENSP00000483537.1:n.*2-9036G>A
|
|
ENST00000638786.2:n.1612C>T
(ATM)
|
|
|
ENST00000675595.1:c.*4049C>T
(ATM)
|
ENSP00000502563.1:n.*4049C>T
|
|
ENST00000682286.1:n.3671C>T
(ATM)
|
|
|
ENST00000682302.1:n.3332C>T
(ATM)
|
|
|
ENST00000682569.1:n.2261C>T
(ATM)
|
|
|
ENST00000683174.1:n.10398C>T
(ATM)
|
|
|
ENST00000683524.1:n.4138C>T
(ATM)
|
|
|
ENST00000684152.1:n.4330C>T
(ATM)
|
|
|
ENST00000684180.1:n.1388C>T
(ATM)
|
|
|
ENST00000684447.1:n.5407C>T
(ATM)
|
|
|
ENST00000713593.1:c.*8385C>T
(ATM)
|
ENSP00000518889.1:n.*8385C>T
|
|
XM_005271414.3:c.787+20775G>A
(C11orf65)
|
XP_005271471.1:n.787+20775G>A
|
|
XM_005271414.4:c.787+20775G>A
(C11orf65)
|
XP_005271471.1:n.787+20775G>A
|
|
XM_005271415.3:c.731+28063G>A
(C11orf65)
|
XP_005271472.1:n.731+28063G>A
|
|
XM_005271415.4:c.731+28063G>A
(C11orf65)
|
XP_005271472.1:n.731+28063G>A
|
|
XM_005271561.3:c.8914C>T
(ATM)
|
XP_005271618.2:p.Gln2972Ter
|
|
XM_005271562.3:c.8914C>T
(ATM)
|
XP_005271619.2:p.Gln2972Ter
|
|
XM_005271562.5:c.8914C>T
(ATM)
|
XP_005271619.2:p.Gln2972Ter
|
|
XM_006718843.2:c.8914C>T
(ATM)
|
XP_006718906.1:p.Gln2972Ter
|
|
XM_006718843.4:c.8914C>T
(ATM)
|
XP_006718906.1:p.Gln2972Ter
|
|
XM_006718845.1:c.4870C>T
(ATM)
|
XP_006718908.1:p.Gln1624Ter
|
|
XM_006718845.2:c.4870C>T
(ATM)
|
XP_006718908.1:p.Gln1624Ter
|
|
XM_011542640.1:c.787+20775G>A
(C11orf65)
|
XP_011540942.1:n.787+20775G>A
|
|
XM_011542640.2:c.787+20775G>A
(C11orf65)
|
XP_011540942.1:n.787+20775G>A
|
|
XM_011542642.1:c.732-16072G>A
(C11orf65)
|
XP_011540944.1:n.732-16072G>A
|
|
XM_011542643.1:c.732-24781G>A
(C11orf65)
|
XP_011540945.1:n.732-24781G>A
|
|
XM_011542643.2:c.732-24781G>A
(C11orf65)
|
XP_011540945.1:n.732-24781G>A
|
|
XM_011542840.1:c.8914C>T
(ATM)
|
XP_011541142.1:p.Gln2972Ter
|
|
XM_011542840.3:c.8914C>T
(ATM)
|
XP_011541142.1:p.Gln2972Ter
|
|
XM_011542841.1:c.8914C>T
(ATM)
|
XP_011541143.1:p.Gln2972Ter
|
|
XM_011542842.1:c.8749C>T
(ATM)
|
XP_011541144.1:p.Gln2917Ter
|
|
XM_011542842.3:c.8749C>T
(ATM)
|
XP_011541144.1:p.Gln2917Ter
|
|
XM_011542844.1:c.7870C>T
(ATM)
|
XP_011541146.1:p.Gln2624Ter
|
|
XM_011542844.3:c.7870C>T
(ATM)
|
XP_011541146.1:p.Gln2624Ter
|
|
XM_011542845.1:c.7606C>T
(ATM)
|
XP_011541147.1:p.Gln2536Ter
|
|
XM_011542845.2:c.7606C>T
(ATM)
|
XP_011541147.1:p.Gln2536Ter
|
|
XM_011542847.1:c.3985C>T
(ATM)
|
XP_011541149.1:p.Gln1329Ter
|
|
XM_017017247.1:c.903+17915G>A
(C11orf65)
|
XP_016872736.1:n.903+17915G>A
|
|
XM_017017789.2:c.8914C>T
(ATM)
|
XP_016873278.1:p.Gln2972Ter
|
|
XM_017017790.2:c.8914C>T
(ATM)
|
XP_016873279.1:p.Gln2972Ter
|
