ENST00000312251.8:c.920+166G>T
MANE Select
|
ENSP00000310998.3:n.920+166G>T
|
|
ENST00000649828.1:c.920+166G>T
|
ENSP00000498032.1:n.920+166G>T
|
|
ENST00000312251.7:c.920+166G>T
|
ENSP00000310998.3:n.920+166G>T
|
|
ENST00000381955.7:c.920+166G>T
|
ENSP00000371381.3:n.920+166G>T
|
|
ENST00000562346.2:c.505-529G>T
|
|
|
ENST00000562746.5:c.920+166G>T
|
ENSP00000455900.1:n.920+166G>T
|
|
ENST00000563578.5:c.738+166G>T
|
|
|
ENST00000564397.5:n.1445G>T
|
|
|
ENST00000565876.5:c.481-1335G>T
|
|
|
ENST00000567739.5:n.239+166G>T
|
|
|
ENST00000568202.5:n.783+166G>T
|
|
|
ENST00000569296.5:c.464+166G>T
|
ENSP00000465949.1:n.464+166G>T
|
|
NM_016256.3:c.920+166G>T
|
NP_057340.2:n.920+166G>T
|
|
XM_011522517.1:c.920+166G>T
|
XP_011520819.1:n.920+166G>T
|
|
XM_011522518.1:c.920+166G>T
|
XP_011520820.1:n.920+166G>T
|
|
XM_011522519.1:c.920+166G>T
|
XP_011520821.1:n.920+166G>T
|
|
XR_243285.1:n.947+166G>T
|
|
|
XM_011522517.3:c.920+166G>T
|
XP_011520819.1:n.920+166G>T
|
|
XR_001751908.2:n.946+166G>T
|
|
|
XR_001751909.2:n.946+166G>T
|
|
|
XR_001751910.2:n.946+166G>T
|
|
|
XR_001751911.2:n.946+166G>T
|
|
|
XR_001751912.2:n.946+166G>T
|
|
|
NM_016256.4:c.920+166G>T
MANE Select
|
NP_057340.2:n.920+166G>T
|
|