ENST00000262304.9:c.7290A>T
MANE Select
|
ENSP00000262304.4:p.Arg2430=
|
|
ENST00000262304.8:c.7290A>T
|
ENSP00000262304.4:p.Arg2430=
|
|
ENST00000415938.7:n.535A>T
|
|
|
ENST00000423118.5:c.7290A>T
|
ENSP00000399501.1:p.Arg2430=
|
|
ENST00000483024.1:c.458A>T
|
|
|
ENST00000483558.5:n.349A>T
|
|
|
ENST00000483731.5:n.1015A>T
|
|
|
ENST00000486339.6:n.1036A>T
|
|
|
ENST00000487932.5:c.1977A>T
|
ENSP00000457132.1:p.Arg659=
|
|
ENST00000496574.6:n.1293A>T
|
|
|
ENST00000565639.6:n.998A>T
|
|
|
ENST00000568591.5:c.2451A>T
|
ENSP00000457162.1:n.2451A>T
|
|
ENST00000569983.5:n.646A>T
|
|
|
NM_000296.3:c.7290A>T
|
NP_000287.3:p.Arg2430=
|
|
NM_001009944.2:c.7290A>T
|
NP_001009944.2:p.Arg2430=
|
|
XM_005255370.2:c.4245A>T
|
XP_005255427.1:p.Arg1415=
|
|
XM_011522525.1:c.7368A>T
|
XP_011520827.1:p.Arg2456=
|
|
XM_011522526.1:c.7368A>T
|
XP_011520828.1:p.Arg2456=
|
|
XM_011522527.1:c.7368A>T
|
XP_011520829.1:p.Arg2456=
|
|
XM_011522528.1:c.7344A>T
|
XP_011520830.1:p.Arg2448=
|
|
XM_011522529.1:c.7344A>T
|
XP_011520831.1:p.Arg2448=
|
|
XM_011522530.1:c.7314A>T
|
XP_011520832.1:p.Arg2438=
|
|
XM_011522531.1:c.7296A>T
|
XP_011520833.1:p.Arg2432=
|
|
XM_011522532.1:c.7242A>T
|
XP_011520834.1:p.Arg2414=
|
|
XM_011522533.1:c.7161A>T
|
XP_011520835.1:p.Arg2387=
|
|
XM_011522534.1:c.7104A>T
|
XP_011520836.1:p.Arg2368=
|
|
XM_011522535.1:c.5190A>T
|
XP_011520837.1:p.Arg1730=
|
|
XM_011522536.1:c.7368A>T
|
XP_011520838.1:p.Arg2456=
|
|
XM_011522537.1:c.4368A>T
|
XP_011520839.1:p.Arg1456=
|
|
XR_932867.1:n.7383A>T
|
|
|
XR_932868.1:n.7383A>T
|
|
|
XR_932869.1:n.7383A>T
|
|
|
XR_932870.1:n.7383A>T
|
|
|
XM_005255370.3:c.4245A>T
|
XP_005255427.1:p.Arg1415=
|
|
XM_011522528.3:c.7344A>T
|
XP_011520830.1:p.Arg2448=
|
|
XM_011522529.2:c.7344A>T
|
XP_011520831.1:p.Arg2448=
|
|
XM_011522537.2:c.4368A>T
|
XP_011520839.1:p.Arg1456=
|
|
XM_024450298.1:c.7410A>T
|
XP_024306066.1:p.Arg2470=
|
|
XM_024450299.1:c.7338A>T
|
XP_024306067.1:p.Arg2446=
|
|
XM_024450300.1:c.7200A>T
|
XP_024306068.1:p.Arg2400=
|
|
XM_024450301.1:c.5286A>T
|
XP_024306069.1:p.Arg1762=
|
|
NM_000296.4:c.7290A>T
|
NP_000287.4:p.Arg2430=
|
|
NM_001009944.3:c.7290A>T
MANE Select
|
NP_001009944.3:p.Arg2430=
|
|