NM_006745.5:c.405-161C>T
MANE Select
|
NP_006736.1:n.405-161C>T
|
ENST00000261507.11:c.405-161C>T
MANE Select
|
ENSP00000261507.6:n.405-161C>T
|
NM_001017369.2:c.12-161C>T
|
NP_001017369.1:n.12-161C>T
|
NM_001017369.3:c.12-161C>T
|
NP_001017369.1:n.12-161C>T
|
NM_006745.4:c.405-161C>T
|
NP_006736.1:n.405-161C>T
|
ENST00000261507.10:c.405-161C>T
|
ENSP00000261507.6:n.405-161C>T
|
ENST00000393766.6:c.12-161C>T
|
ENSP00000377361.2:n.12-161C>T
|
ENST00000504317.1:c.405-161C>T
|
ENSP00000423633.1:n.405-161C>T
|
ENST00000507013.5:c.405-161C>T
|
ENSP00000425241.1:n.405-161C>T
|
XM_005263176.1:c.405-161C>T
|
XP_005263233.1:n.405-161C>T
|
XM_005263176.2:c.405-161C>T
|
XP_005263233.1:n.405-161C>T
|