|
ENST00000452508.7:c.7923G>T
(ATM)
|
ENSP00000388058.2:p.Gln2641His
|
|
|
ENST00000713593.1:c.*7394G>T
(ATM)
|
ENSP00000518889.1:n.*7394G>T
|
|
|
ENST00000278616.9:c.7923G>T
(ATM)
|
ENSP00000278616.4:p.Gln2641His
|
|
|
ENST00000525056.2:n.2342G>T
(ATM)
|
|
|
|
ENST00000525537.3:n.1604G>T
(ATM)
|
|
|
|
ENST00000638786.2:n.625+859G>T
(ATM)
|
|
|
|
ENST00000682286.1:n.2680G>T
(ATM)
|
|
|
|
ENST00000682302.1:n.2341G>T
(ATM)
|
|
|
|
ENST00000683174.1:n.9407G>T
(ATM)
|
|
|
|
ENST00000683524.1:n.3147G>T
(ATM)
|
|
|
|
ENST00000684152.1:n.3344-990G>T
(ATM)
|
|
|
|
ENST00000684180.1:n.397G>T
(ATM)
|
|
|
|
ENST00000684447.1:n.3431G>T
(ATM)
|
|
|
|
ENST00000527805.6:c.*2987G>T
(ATM)
|
ENSP00000435747.2:n.*2987G>T
|
|
|
ENST00000675595.1:c.*3058G>T
(ATM)
|
ENSP00000502563.1:n.*3058G>T
|
|
|
ENST00000675843.1:c.7923G>T
(ATM)
MANE Select
|
ENSP00000501606.1:p.Gln2641His
|
|
|
ENST00000278616.8:c.7923G>T
(ATM)
|
ENSP00000278616.4:p.Gln2641His
|
|
|
ENST00000452508.6:c.7923G>T
(ATM)
|
ENSP00000388058.2:p.Gln2641His
|
|
|
ENST00000524755.5:c.300-1329C>A
(C11orf65)
|
|
|
|
ENST00000524792.5:n.4138G>T
(ATM)
|
|
|
|
ENST00000525056.1:n.120G>T
(ATM)
|
|
|
|
ENST00000525729.5:c.641-23825C>A
(C11orf65)
|
ENSP00000433395.1:n.641-23825C>A
|
|
|
ENST00000527531.5:c.*1270-1329C>A
(C11orf65)
|
ENSP00000431706.1:n.*1270-1329C>A
|
|
|
ENST00000533690.5:n.3327G>T
(ATM)
|
|
|
|
ENST00000533979.5:n.135G>T
(ATM)
|
|
|
|
ENST00000615746.4:c.*1270-1329C>A
(C11orf65)
|
ENSP00000483537.1:n.*1270-1329C>A
|
|
|
NM_000051.3:c.7923G>T , LRG_135t1:c.7923G>T
(ATM)
|
NP_000042.3:p.Gln2641His
|
|
|
XM_005271414.3:c.*39-1329C>A
(C11orf65)
|
XP_005271471.1:n.*39-1329C>A
|
|
|
XM_005271415.3:c.805-1329C>A
(C11orf65)
|
XP_005271472.1:n.805-1329C>A
|
|
|
XM_005271561.3:c.7923G>T
(ATM)
|
XP_005271618.2:p.Gln2641His
|
|
|
XM_005271562.3:c.7923G>T
(ATM)
|
XP_005271619.2:p.Gln2641His
|
|
|
XM_006718843.2:c.7923G>T
(ATM)
|
XP_006718906.1:p.Gln2641His
|
|
|
XM_006718845.1:c.3879G>T
(ATM)
|
XP_006718908.1:p.Gln1293His
|
|
|
XM_011542840.1:c.7923G>T
(ATM)
|
XP_011541142.1:p.Gln2641His
|
|
|
XM_011542841.1:c.7923G>T
(ATM)
|
XP_011541143.1:p.Gln2641His
|
|
|
XM_011542842.1:c.7758G>T
(ATM)
|
XP_011541144.1:p.Gln2586His
|
|
|
XM_011542843.1:c.7923G>T
(ATM)
|
XP_011541145.1:p.Gln2641His
|
|
|
XM_011542844.1:c.6879G>T
(ATM)
|
XP_011541146.1:p.Gln2293His
|
|
|
XM_011542845.1:c.6615G>T
(ATM)
|
XP_011541147.1:p.Gln2205His
|
|
|
XM_011542847.1:c.2994G>T
(ATM)
|
XP_011541149.1:p.Gln998His
|
|
|
NM_001330368.1:c.641-23825C>A
(C11orf65)
|
NP_001317297.1:n.641-23825C>A
|
|
|
NM_001351110.1:c.*38+2324C>A
(C11orf65)
|
NP_001338039.1:n.*38+2324C>A
|
|
|
NM_001351834.1:c.7923G>T
(ATM)
|
NP_001338763.1:p.Gln2641His
|
|
|
NR_147053.2:n.2375-1329C>A
(C11orf65)
|
|
|
|
XM_005271414.4:c.*39-1329C>A
(C11orf65)
|
XP_005271471.1:n.*39-1329C>A
|
|
|
XM_005271415.4:c.805-1329C>A
(C11orf65)
|
XP_005271472.1:n.805-1329C>A
|
|
|
XM_005271562.5:c.7923G>T
(ATM)
|
XP_005271619.2:p.Gln2641His
|
|
|
XM_006718843.4:c.7923G>T
(ATM)
|
XP_006718906.1:p.Gln2641His
|
|
|
XM_006718845.2:c.3879G>T
(ATM)
|
XP_006718908.1:p.Gln1293His
|
|
|
XM_011542840.3:c.7923G>T
(ATM)
|
XP_011541142.1:p.Gln2641His
|
|
|
XM_011542842.3:c.7758G>T
(ATM)
|
XP_011541144.1:p.Gln2586His
|
|
|
XM_011542843.2:c.7923G>T
(ATM)
|
XP_011541145.1:p.Gln2641His
|
|
|
XM_011542844.3:c.6879G>T
(ATM)
|
XP_011541146.1:p.Gln2293His
|
|
|
XM_011542845.2:c.6615G>T
(ATM)
|
XP_011541147.1:p.Gln2205His
|
|
|
XM_017017789.2:c.7923G>T
(ATM)
|
XP_016873278.1:p.Gln2641His
|
|
|
XM_017017790.2:c.7923G>T
(ATM)
|
XP_016873279.1:p.Gln2641His
|
|
|
NM_001330368.2:c.641-23825C>A
(C11orf65)
|
NP_001317297.1:n.641-23825C>A
|
|
|
NM_001351110.2:c.*38+2324C>A
(C11orf65)
|
NP_001338039.1:n.*38+2324C>A
|
|
|
NM_001351834.2:c.7923G>T
(ATM)
|
NP_001338763.1:p.Gln2641His
|
|
|
NM_000051.4:c.7923G>T
(ATM)
MANE Select
|
NP_000042.3:p.Gln2641His
|
|
|
NR_147053.3:n.2373-1329C>A
(C11orf65)
|
|
|
