|
NM_001009944.3:c.12448C>T
MANE Select
|
NP_001009944.3:p.Arg4150Cys
|
|
ENST00000262304.9:c.12448C>T
MANE Select
|
ENSP00000262304.4:p.Arg4150Cys
|
|
NM_000296.3:c.12445C>T
|
NP_000287.3:p.Arg4149Cys
|
|
NM_000296.4:c.12445C>T
|
NP_000287.4:p.Arg4149Cys
|
|
NM_001009944.2:c.12448C>T
|
NP_001009944.2:p.Arg4150Cys
|
|
ENST00000262304.8:c.12448C>T
|
ENSP00000262304.4:p.Arg4150Cys
|
|
ENST00000423118.5:c.12445C>T
|
ENSP00000399501.1:p.Arg4149Cys
|
|
ENST00000472577.1:n.476C>T
|
|
|
XM_005255370.2:c.9403C>T
|
XP_005255427.1:p.Arg3135Cys
|
|
XM_005255370.3:c.9403C>T
|
XP_005255427.1:p.Arg3135Cys
|
|
XM_011522525.1:c.12526C>T
|
XP_011520827.1:p.Arg4176Cys
|
|
XM_011522526.1:c.12523C>T
|
XP_011520828.1:p.Arg4175Cys
|
|
XM_011522527.1:c.12508C>T
|
XP_011520829.1:p.Arg4170Cys
|
|
XM_011522528.1:c.12502C>T
|
XP_011520830.1:p.Arg4168Cys
|
|
XM_011522528.3:c.12502C>T
|
XP_011520830.1:p.Arg4168Cys
|
|
XM_011522529.1:c.12499C>T
|
XP_011520831.1:p.Arg4167Cys
|
|
XM_011522529.2:c.12499C>T
|
XP_011520831.1:p.Arg4167Cys
|
|
XM_011522530.1:c.12472C>T
|
XP_011520832.1:p.Arg4158Cys
|
|
XM_011522531.1:c.12454C>T
|
XP_011520833.1:p.Arg4152Cys
|
|
XM_011522532.1:c.12400C>T
|
XP_011520834.1:p.Arg4134Cys
|
|
XM_011522533.1:c.12319C>T
|
XP_011520835.1:p.Arg4107Cys
|
|
XM_011522534.1:c.12262C>T
|
XP_011520836.1:p.Arg4088Cys
|
|
XM_011522535.1:c.10348C>T
|
XP_011520837.1:p.Arg3450Cys
|
|
XM_011522537.1:c.9526C>T
|
XP_011520839.1:p.Arg3176Cys
|
|
XM_011522537.2:c.9526C>T
|
XP_011520839.1:p.Arg3176Cys
|
|
XM_024450298.1:c.12568C>T
|
XP_024306066.1:p.Arg4190Cys
|
|
XM_024450299.1:c.12496C>T
|
XP_024306067.1:p.Arg4166Cys
|
|
XM_024450300.1:c.12358C>T
|
XP_024306068.1:p.Arg4120Cys
|
|
XM_024450301.1:c.10444C>T
|
XP_024306069.1:p.Arg3482Cys
|
|
XR_932867.1:n.12366C>T
|
|
