|
NM_002334.4:c.3699+1G>A
MANE Select
|
NP_002325.2:n.3699+1G>A
|
|
ENST00000378623.6:c.3699+1G>A
MANE Select
|
ENSP00000367888.1:n.3699+1G>A
|
|
NM_002334.3:c.3699+1G>A
|
NP_002325.2:n.3699+1G>A
|
|
ENST00000378623.5:c.3699+1G>A
|
ENSP00000367888.1:n.3699+1G>A
|
|
XM_011520102.1:c.3912+1G>A
|
XP_011518404.1:n.3912+1G>A
|
|
XM_011520103.1:c.2895+1G>A
|
XP_011518405.1:n.2895+1G>A
|
|
XM_011520103.2:c.2895+1G>A
|
XP_011518405.1:n.2895+1G>A
|
|
XM_011520104.1:c.1464+1G>A
|
XP_011518406.1:n.1464+1G>A
|
|
XM_011520104.2:c.1464+1G>A
|
XP_011518406.1:n.1464+1G>A
|
|
XM_017017734.1:c.3699+1G>A
|
XP_016873223.1:n.3699+1G>A
|