ENST00000261304.7:c.*1340G>T
MANE Select
|
ENSP00000261304.2:n.*1340G>T
|
|
ENST00000261304.6:c.*1340G>T
|
ENSP00000261304.2:n.*1340G>T
|
|
ENST00000555000.5:c.*74+507G>T
|
ENSP00000450472.1:n.*74+507G>T
|
|
NM_000153.3:c.*1340G>T
|
NP_000144.2:n.*1340G>T
|
|
NM_001201401.1:c.*1340G>T
|
NP_001188330.1:n.*1340G>T
|
|
NM_001201402.1:c.*1340G>T
|
NP_001188331.1:n.*1340G>T
|
|
XM_011536618.1:c.*1340G>T
|
XP_011534920.1:n.*1340G>T
|
|
XM_011536618.2:c.*1340G>T
|
XP_011534920.1:n.*1340G>T
|
|
NM_000153.4:c.*1340G>T
MANE Select
|
NP_000144.2:n.*1340G>T
|
|
NM_001201401.2:c.*1340G>T
|
NP_001188330.1:n.*1340G>T
|
|
NM_001201402.2:c.*1340G>T
|
NP_001188331.1:n.*1340G>T
|
|