ENST00000375448.4:c.1048-146C>T
MANE Select
|
ENSP00000364597.4:n.1048-146C>T
|
|
ENST00000468945.1:n.107-146C>T
|
|
|
NM_012387.2:c.1048-146C>T
|
NP_036519.2:n.1048-146C>T
|
|
XM_011541150.1:c.862-146C>T
|
XP_011539452.1:n.862-146C>T
|
|
XM_011541151.1:c.1048-146C>T
|
XP_011539453.1:n.1048-146C>T
|
|
XM_011541152.1:c.511-146C>T
|
XP_011539454.1:n.511-146C>T
|
|
XM_011541153.1:c.1048-146C>T
|
XP_011539455.1:n.1048-146C>T
|
|
XM_011541154.1:c.1048-146C>T
|
XP_011539456.1:n.1048-146C>T
|
|
XM_011541155.1:c.1048-146C>T
|
XP_011539457.1:n.1048-146C>T
|
|
XM_011541156.1:c.1048-146C>T
|
XP_011539458.1:n.1048-146C>T
|
|
XM_011541157.1:c.157-146C>T
|
XP_011539459.1:n.157-146C>T
|
|
XM_011541154.2:c.1048-146C>T
|
XP_011539456.1:n.1048-146C>T
|
|
NM_012387.3:c.1048-146C>T
MANE Select
|
NP_036519.2:n.1048-146C>T
|
|