|
ENST00000336079.8:c.*1076dup
MANE Select
|
ENSP00000336725.3:n.*1076dup
|
|
|
ENST00000336079.7:c.*1076dup
|
ENSP00000336725.3:n.*1076dup
|
|
|
NM_004660.4:c.*1076dup
|
NP_004651.2:n.*1076dup
|
|
|
XM_006724878.1:c.*1076dup
|
XP_006724941.1:n.*1076dup
|
|
|
NM_001122665.3:c.*1076dup
|
NP_001116137.1:n.*1076dup
|
|
|
NM_001302552.2:c.*1076dup
|
NP_001289481.1:n.*1076dup
|
|
|
NM_001324195.1:c.*1076dup
|
NP_001311124.1:n.*1076dup
|
|
|
NR_136716.1:n.3528dup
|
|
|
|
NR_136717.1:n.3290dup
|
|
|
|
NR_136718.1:n.3608dup
|
|
|
|
NR_136719.1:n.3398dup
|
|
|
|
NR_136720.1:n.3459dup
|
|
|
|
NR_136721.1:n.3121dup
|
|
|
|
NR_136722.1:n.3205dup
|
|
|
|
NR_136723.1:n.3523dup
|
|
|
|
NR_136724.1:n.3443dup
|
|
|
|
XR_001756014.2:n.3223dup
|
|
|
|
NM_004660.5:c.*1076dup
MANE Select
|
NP_004651.2:n.*1076dup
|
|
|
NM_001302552.3:c.*1076dup
|
NP_001289481.1:n.*1076dup
|
|
|
NM_001324195.2:c.*1076dup
|
NP_001311124.1:n.*1076dup
|
|
|
NR_136716.2:n.3446dup
|
|
|
|
NR_136717.2:n.3208dup
|
|
|
|
NR_136718.2:n.3526dup
|
|
|
|
NR_136719.2:n.3316dup
|
|
|
|
NR_136720.2:n.3377dup
|
|
|
|
NR_136721.2:n.3111dup
|
|
|
