ENST00000378823.8:c.3389+294G>T
MANE Select
|
ENSP00000368100.4:n.3389+294G>T
|
|
ENST00000638452.2:c.3092+294G>T
|
ENSP00000492349.2:n.3092+294G>T
|
|
ENST00000638504.1:n.2997+294G>T
|
|
|
ENST00000638568.2:c.3092+294G>T
|
ENSP00000491158.2:n.3092+294G>T
|
|
ENST00000639899.1:n.3908+294G>T
|
|
|
ENST00000640655.2:c.3092+294G>T
|
ENSP00000491596.2:n.3092+294G>T
|
|
ENST00000651249.1:c.225+294G>T
|
|
|
ENST00000378823.7:c.3389+294G>T
|
ENSP00000368100.4:n.3389+294G>T
|
|
ENST00000455677.1:c.24+294G>T
|
|
|
ENST00000533482.5:c.*3015+294G>T
|
ENSP00000431225.1:n.*3015+294G>T
|
|
NM_005732.3:c.3389+294G>T
|
NP_005723.2:n.3389+294G>T
|
|
NM_005732.4:c.3389+294G>T
MANE Select
|
NP_005723.2:n.3389+294G>T
|
|