ENST00000271324.6:c.-18+1888T>G
MANE Select
|
ENSP00000271324.5:n.-18+1888T>G
|
|
ENST00000648608.1:c.-18+1888T>G
|
ENSP00000497382.1:n.-18+1888T>G
|
|
ENST00000271324.5:c.-18+1888T>G
|
ENSP00000271324.5:n.-18+1888T>G
|
|
ENST00000471220.5:n.66+1888T>G
|
|
|
NM_000560.3:c.-18+1888T>G
|
NP_000551.1:n.-18+1888T>G
|
|
NM_001040033.1:c.-18+1888T>G
|
NP_001035122.1:n.-18+1888T>G
|
|
XM_006711053.2:c.-18+1888T>G
|
XP_006711116.1:n.-18+1888T>G
|
|
XM_011542447.1:c.-18+1888T>G
|
XP_011540749.1:n.-18+1888T>G
|
|
NM_001320638.1:c.-18+1888T>G
|
NP_001307567.1:n.-18+1888T>G
|
|
XM_024451057.1:c.-894+1888T>G
|
XP_024306825.1:n.-894+1888T>G
|
|
NM_000560.4:c.-18+1888T>G
MANE Select
|
NP_000551.1:n.-18+1888T>G
|
|
NM_001040033.2:c.-18+1888T>G
|
NP_001035122.1:n.-18+1888T>G
|
|
NM_001320638.2:c.-18+1888T>G
|
NP_001307567.1:n.-18+1888T>G
|
|