ENST00000371696.7:c.588+69G>T
MANE Select
|
ENSP00000360761.2:n.588+69G>T
|
|
ENST00000371694.7:c.492+445G>T
|
ENSP00000360759.3:n.492+445G>T
|
|
ENST00000371696.6:c.588+69G>T
|
ENSP00000360761.2:n.588+69G>T
|
|
ENST00000472820.1:n.516+69G>T
|
|
|
ENST00000538402.1:c.588+69G>T
|
ENSP00000438919.1:n.588+69G>T
|
|
NM_001012727.1:c.492+445G>T
|
NP_001012745.1:n.492+445G>T
|
|
NM_006412.3:c.588+69G>T
|
NP_006403.2:n.588+69G>T
|
|
NM_006412.4:c.588+69G>T
MANE Select
|
NP_006403.2:n.588+69G>T
|
|
NM_001012727.2:c.492+445G>T
|
NP_001012745.1:n.492+445G>T
|
|