ENST00000378823.8:c.-326G>T
MANE Select
|
ENSP00000368100.4:n.-326G>T
|
|
ENST00000638452.2:c.-168-2285G>T
|
ENSP00000492349.2:n.-168-2285G>T
|
|
ENST00000638504.1:n.207-2285G>T
|
|
|
ENST00000638568.2:c.-169+526G>T
|
ENSP00000491158.2:n.-169+526G>T
|
|
ENST00000639899.1:n.290-2285G>T
|
|
|
ENST00000640655.2:c.-168-2285G>T
|
ENSP00000491596.2:n.-168-2285G>T
|
|
ENST00000651160.1:c.-326G>T
|
ENSP00000498829.1:n.-326G>T
|
|
ENST00000651541.1:c.-179G>T
|
ENSP00000498795.1:n.-179G>T
|
|
ENST00000652016.1:c.-326G>T
|
ENSP00000498267.1:n.-326G>T
|
|
ENST00000652485.1:c.-326G>T
|
ENSP00000498973.1:n.-326G>T
|
|
ENST00000378823.7:c.-326G>T
|
ENSP00000368100.4:n.-326G>T
|
|
ENST00000416135.5:c.-169+526G>T
|
ENSP00000389515.1:n.-169+526G>T
|
|
ENST00000533482.5:c.-326G>T
|
ENSP00000431225.1:n.-326G>T
|
|
NM_005732.3:c.-326G>T
|
NP_005723.2:n.-326G>T
|
|
NM_005732.4:c.-326G>T
MANE Select
|
NP_005723.2:n.-326G>T
|
|