ENST00000372396.4:c.-40+1083G>T
MANE Select
|
ENSP00000361473.3:n.-40+1083G>T
|
|
ENST00000645057.1:c.-40+1083G>T
|
ENSP00000494063.1:n.-40+1083G>T
|
|
ENST00000372396.3:c.-40+1083G>T
|
ENSP00000361473.3:n.-40+1083G>T
|
|
ENST00000463151.5:n.139+661G>T
|
|
|
NM_014663.2:c.-40+1083G>T
|
NP_055478.2:n.-40+1083G>T
|
|
XM_005271354.2:c.-40+661G>T
|
XP_005271411.1:n.-40+661G>T
|
|
XM_005271355.2:c.-40+786G>T
|
XP_005271412.1:n.-40+786G>T
|
|
XM_005271356.2:c.-450+786G>T
|
XP_005271413.1:n.-450+786G>T
|
|
XM_005271354.3:c.-40+661G>T
|
XP_005271411.1:n.-40+661G>T
|
|
XM_005271355.3:c.-40+786G>T
|
XP_005271412.1:n.-40+786G>T
|
|
NM_014663.3:c.-40+1083G>T
MANE Select
|
NP_055478.2:n.-40+1083G>T
|
|