ENST00000253788.12:c.-3+13T>C
MANE Select
|
ENSP00000253788.5:n.-3+13T>C
|
|
ENST00000589913.6:c.-267T>C
|
ENSP00000464813.1:n.-267T>C
|
|
ENST00000253788.9:c.-3+13T>C
|
ENSP00000253788.4:n.-3+13T>C
|
|
ENST00000587478.1:n.53+13T>C
|
|
|
ENST00000588830.1:c.-3+13T>C
|
ENSP00000468468.1:n.-3+13T>C
|
|
ENST00000589037.5:c.-3+69T>C
|
ENSP00000467587.1:n.-3+69T>C
|
|
ENST00000589913.5:c.-267T>C
|
ENSP00000464813.1:n.-267T>C
|
|
ENST00000593262.1:n.66T>C
|
|
|
NM_000988.3:c.-3+13T>C
|
NP_000979.1:n.-3+13T>C
|
|
NM_000988.5:c.-3+13T>C
MANE Select
|
NP_000979.1:n.-3+13T>C
|
|
NM_001349921.1:c.-3+69T>C
|
NP_001336850.1:n.-3+69T>C
|
|
NM_001349922.1:c.-267T>C
|
NP_001336851.1:n.-267T>C
|
|
NR_146327.1:n.81+13T>C
|
|
|
NM_001349921.2:c.-3+69T>C
|
NP_001336850.1:n.-3+69T>C
|
|
NM_001349922.2:c.-267T>C
|
NP_001336851.1:n.-267T>C
|
|
NR_146327.2:n.53+13T>C
|
|
|