ENST00000452508.7:c.7194C=
(ATM)
|
ENSP00000388058.2:p.Tyr2398=
|
|
ENST00000713593.1:c.*6665C=
(ATM)
|
ENSP00000518889.1:n.*6665C=
|
|
ENST00000278616.9:c.7194C=
(ATM)
|
ENSP00000278616.4:p.Tyr2398=
|
|
ENST00000525056.2:n.1613C=
(ATM)
|
|
|
ENST00000525537.3:n.151C=
(ATM)
|
|
|
ENST00000638786.2:n.31C=
(ATM)
|
|
|
ENST00000682286.1:n.1951C=
(ATM)
|
|
|
ENST00000682302.1:n.1612C=
(ATM)
|
|
|
ENST00000683174.1:n.8678C=
(ATM)
|
|
|
ENST00000683524.1:n.2418C=
(ATM)
|
|
|
ENST00000684152.1:n.2908C=
(ATM)
|
|
|
ENST00000684447.1:n.1657C=
(ATM)
|
|
|
ENST00000527805.6:c.*2258C=
(ATM)
|
ENSP00000435747.2:n.*2258C=
|
|
ENST00000675595.1:c.*2329C=
(ATM)
|
ENSP00000502563.1:n.*2329C=
|
|
ENST00000675843.1:c.7194C=
(ATM)
MANE Select
|
ENSP00000501606.1:p.Tyr2398=
|
|
ENST00000278616.8:c.7194C=
(ATM)
|
ENSP00000278616.4:p.Tyr2398=
|
|
ENST00000452508.6:c.7194C=
(ATM)
|
ENSP00000388058.2:p.Tyr2398=
|
|
ENST00000524792.5:n.3409C=
(ATM)
|
|
|
ENST00000525537.2:n.470C=
(ATM)
|
|
|
ENST00000525729.5:c.641-20054G=
(C11orf65)
|
ENSP00000433395.1:n.641-20054G=
|
|
ENST00000527389.2:n.219C=
(ATM)
|
|
|
ENST00000533690.5:n.2598C=
(ATM)
|
|
|
NM_000051.3:c.7194C= , LRG_135t1:c.7194C=
(ATM)
|
NP_000042.3:p.Tyr2398=
|
|
XM_005271561.3:c.7194C=
(ATM)
|
XP_005271618.2:p.Tyr2398=
|
|
XM_005271562.3:c.7194C=
(ATM)
|
XP_005271619.2:p.Tyr2398=
|
|
XM_006718843.2:c.7194C=
(ATM)
|
XP_006718906.1:p.Tyr2398=
|
|
XM_006718845.1:c.3150C=
(ATM)
|
XP_006718908.1:p.Tyr1050=
|
|
XM_011542840.1:c.7194C=
(ATM)
|
XP_011541142.1:p.Tyr2398=
|
|
XM_011542841.1:c.7194C=
(ATM)
|
XP_011541143.1:p.Tyr2398=
|
|
XM_011542842.1:c.7029C=
(ATM)
|
XP_011541144.1:p.Tyr2343=
|
|
XM_011542843.1:c.7194C=
(ATM)
|
XP_011541145.1:p.Tyr2398=
|
|
XM_011542844.1:c.6150C=
(ATM)
|
XP_011541146.1:p.Tyr2050=
|
|
XM_011542845.1:c.5886C=
(ATM)
|
XP_011541147.1:p.Tyr1962=
|
|
XM_011542847.1:c.2265C=
(ATM)
|
XP_011541149.1:p.Tyr755=
|
|
NM_001330368.1:c.641-20054G=
(C11orf65)
|
NP_001317297.1:n.641-20054G=
|
|
NM_001351110.1:c.*38+6095G=
(C11orf65)
|
NP_001338039.1:n.*38+6095G=
|
|
NM_001351834.1:c.7194C=
(ATM)
|
NP_001338763.1:p.Tyr2398=
|
|
XM_005271562.5:c.7194C=
(ATM)
|
XP_005271619.2:p.Tyr2398=
|
|
XM_006718843.4:c.7194C=
(ATM)
|
XP_006718906.1:p.Tyr2398=
|
|
XM_006718845.2:c.3150C=
(ATM)
|
XP_006718908.1:p.Tyr1050=
|
|
XM_011542840.3:c.7194C=
(ATM)
|
XP_011541142.1:p.Tyr2398=
|
|
XM_011542842.3:c.7029C=
(ATM)
|
XP_011541144.1:p.Tyr2343=
|
|
XM_011542843.2:c.7194C=
(ATM)
|
XP_011541145.1:p.Tyr2398=
|
|
XM_011542844.3:c.6150C=
(ATM)
|
XP_011541146.1:p.Tyr2050=
|
|
XM_011542845.2:c.5886C=
(ATM)
|
XP_011541147.1:p.Tyr1962=
|
|
XM_017017789.2:c.7194C=
(ATM)
|
XP_016873278.1:p.Tyr2398=
|
|
XM_017017790.2:c.7194C=
(ATM)
|
XP_016873279.1:p.Tyr2398=
|
|
NM_001330368.2:c.641-20054G=
(C11orf65)
|
NP_001317297.1:n.641-20054G=
|
|
NM_001351110.2:c.*38+6095G=
(C11orf65)
|
NP_001338039.1:n.*38+6095G=
|
|
NM_001351834.2:c.7194C=
(ATM)
|
NP_001338763.1:p.Tyr2398=
|
|
NM_000051.4:c.7194C=
(ATM)
MANE Select
|
NP_000042.3:p.Tyr2398=
|
|