ENST00000336079.8:c.*733T>G
MANE Select
|
ENSP00000336725.3:n.*733T>G
|
|
ENST00000336079.7:c.*733T>G
|
ENSP00000336725.3:n.*733T>G
|
|
NM_004660.4:c.*733T>G
|
NP_004651.2:n.*733T>G
|
|
XM_006724878.1:c.*733T>G
|
XP_006724941.1:n.*733T>G
|
|
NM_001122665.3:c.*733T>G
|
NP_001116137.1:n.*733T>G
|
|
NM_001302552.2:c.*733T>G
|
NP_001289481.1:n.*733T>G
|
|
NM_001324195.1:c.*733T>G
|
NP_001311124.1:n.*733T>G
|
|
NR_136716.1:n.3185T>G
|
|
|
NR_136717.1:n.2947T>G
|
|
|
NR_136718.1:n.3265T>G
|
|
|
NR_136719.1:n.3055T>G
|
|
|
NR_136720.1:n.3116T>G
|
|
|
NR_136721.1:n.2778T>G
|
|
|
NR_136722.1:n.2862T>G
|
|
|
NR_136723.1:n.3180T>G
|
|
|
NR_136724.1:n.3100T>G
|
|
|
XR_001756014.2:n.2880T>G
|
|
|
NM_004660.5:c.*733T>G
MANE Select
|
NP_004651.2:n.*733T>G
|
|
NM_001302552.3:c.*733T>G
|
NP_001289481.1:n.*733T>G
|
|
NM_001324195.2:c.*733T>G
|
NP_001311124.1:n.*733T>G
|
|
NR_136716.2:n.3103T>G
|
|
|
NR_136717.2:n.2865T>G
|
|
|
NR_136718.2:n.3183T>G
|
|
|
NR_136719.2:n.2973T>G
|
|
|
NR_136720.2:n.3034T>G
|
|
|
NR_136721.2:n.2768T>G
|
|
|