ENST00000262304.9:c.3445C>T
MANE Select
|
ENSP00000262304.4:p.His1149Tyr
|
|
ENST00000262304.8:c.3445C>T
|
ENSP00000262304.4:p.His1149Tyr
|
|
ENST00000415938.7:n.310+618C>T
|
|
|
ENST00000423118.5:c.3445C>T
|
ENSP00000399501.1:p.His1149Tyr
|
|
ENST00000468674.5:n.430+618C>T
|
|
|
ENST00000469241.2:n.395C>T
|
|
|
ENST00000483024.1:c.233+94C>T
|
|
|
ENST00000483731.5:n.790+618C>T
|
|
|
ENST00000488185.2:c.473-3364C>T
|
|
|
ENST00000565639.6:n.773+618C>T
|
|
|
ENST00000568591.5:c.2226+618C>T
|
ENSP00000457162.1:n.2226+618C>T
|
|
ENST00000569983.5:n.421+618C>T
|
|
|
NM_000296.3:c.3445C>T
|
NP_000287.3:p.His1149Tyr
|
|
NM_001009944.2:c.3445C>T
|
NP_001009944.2:p.His1149Tyr
|
|
XM_005255370.2:c.400C>T
|
XP_005255427.1:p.His134Tyr
|
|
XM_011522525.1:c.3523C>T
|
XP_011520827.1:p.His1175Tyr
|
|
XM_011522526.1:c.3523C>T
|
XP_011520828.1:p.His1175Tyr
|
|
XM_011522527.1:c.3523C>T
|
XP_011520829.1:p.His1175Tyr
|
|
XM_011522528.1:c.3499C>T
|
XP_011520830.1:p.His1167Tyr
|
|
XM_011522529.1:c.3499C>T
|
XP_011520831.1:p.His1167Tyr
|
|
XM_011522530.1:c.3469C>T
|
XP_011520832.1:p.His1157Tyr
|
|
XM_011522531.1:c.3451C>T
|
XP_011520833.1:p.His1151Tyr
|
|
XM_011522532.1:c.3397C>T
|
XP_011520834.1:p.His1133Tyr
|
|
XM_011522533.1:c.3316C>T
|
XP_011520835.1:p.His1106Tyr
|
|
XM_011522534.1:c.3259C>T
|
XP_011520836.1:p.His1087Tyr
|
|
XM_011522535.1:c.1345C>T
|
XP_011520837.1:p.His449Tyr
|
|
XM_011522536.1:c.3523C>T
|
XP_011520838.1:p.His1175Tyr
|
|
XM_011522537.1:c.523C>T
|
XP_011520839.1:p.His175Tyr
|
|
XR_932867.1:n.3538C>T
|
|
|
XR_932868.1:n.3538C>T
|
|
|
XR_932869.1:n.3538C>T
|
|
|
XR_932870.1:n.3538C>T
|
|
|
XM_005255370.3:c.400C>T
|
XP_005255427.1:p.His134Tyr
|
|
XM_011522528.3:c.3499C>T
|
XP_011520830.1:p.His1167Tyr
|
|
XM_011522529.2:c.3499C>T
|
XP_011520831.1:p.His1167Tyr
|
|
XM_011522537.2:c.523C>T
|
XP_011520839.1:p.His175Tyr
|
|
XM_024450298.1:c.3565C>T
|
XP_024306066.1:p.His1189Tyr
|
|
XM_024450299.1:c.3493C>T
|
XP_024306067.1:p.His1165Tyr
|
|
XM_024450300.1:c.3355C>T
|
XP_024306068.1:p.His1119Tyr
|
|
XM_024450301.1:c.1441C>T
|
XP_024306069.1:p.His481Tyr
|
|
NM_000296.4:c.3445C>T
|
NP_000287.4:p.His1149Tyr
|
|
NM_001009944.3:c.3445C>T
MANE Select
|
NP_001009944.3:p.His1149Tyr
|
|