NM_018026.4:c.661-5C>G
MANE Select
|
NP_060496.2:n.661-5C>G
|
ENST00000320580.9:c.661-5C>G
MANE Select
|
ENSP00000316454.4:n.661-5C>G
|
NM_018026.3:c.661-5C>G
|
NP_060496.2:n.661-5C>G
|
ENST00000320580.8:c.661-5C>G
|
ENSP00000316454.4:n.661-5C>G
|
ENST00000527224.1:n.785-5C>G
|
|
ENST00000527380.1:c.367-5C>G
|
ENSP00000432639.1:n.367-5C>G
|
XM_011545162.1:c.340-5C>G
|
XP_011543464.1:n.340-5C>G
|
XM_011545163.1:c.331-5C>G
|
XP_011543465.1:n.331-5C>G
|
XM_011545164.1:c.322-5C>G
|
XP_011543466.1:n.322-5C>G
|
XM_011545164.2:c.322-5C>G
|
XP_011543466.1:n.322-5C>G
|
XR_001747924.1:n.872-5C>G
|
|