ENST00000378823.8:c.-346G>T
MANE Select
|
ENSP00000368100.4:n.-346G>T
|
|
ENST00000638452.2:c.-168-2305G>T
|
ENSP00000492349.2:n.-168-2305G>T
|
|
ENST00000638504.1:n.207-2305G>T
|
|
|
ENST00000638568.2:c.-169+506G>T
|
ENSP00000491158.2:n.-169+506G>T
|
|
ENST00000639899.1:n.290-2305G>T
|
|
|
ENST00000640655.2:c.-168-2305G>T
|
ENSP00000491596.2:n.-168-2305G>T
|
|
ENST00000651541.1:c.-199G>T
|
ENSP00000498795.1:n.-199G>T
|
|
ENST00000652016.1:c.-346G>T
|
ENSP00000498267.1:n.-346G>T
|
|
ENST00000378823.7:c.-346G>T
|
ENSP00000368100.4:n.-346G>T
|
|
ENST00000416135.5:c.-169+506G>T
|
ENSP00000389515.1:n.-169+506G>T
|
|
ENST00000533482.5:c.-346G>T
|
ENSP00000431225.1:n.-346G>T
|
|
NM_005732.3:c.-346G>T
|
NP_005723.2:n.-346G>T
|
|
NM_005732.4:c.-346G>T
MANE Select
|
NP_005723.2:n.-346G>T
|
|