ENST00000373207.2:c.2956G>T
MANE Select
|
ENSP00000362303.1:p.Glu986Ter
|
|
ENST00000373207.1:c.2956G>T
|
ENSP00000362303.1:p.Glu986Ter
|
|
ENST00000373208.5:c.2965G>T
|
ENSP00000362304.1:p.Glu989Ter
|
|
NM_080722.3:c.2956G>T
|
NP_542453.2:p.Glu986Ter
|
|
NM_139155.2:c.2965G>T
|
NP_631894.2:p.Glu989Ter
|
|
XM_011539300.1:c.2455G>T
|
XP_011537602.1:p.Glu819Ter
|
|
XM_011539301.1:c.2029G>T
|
XP_011537603.1:p.Glu677Ter
|
|
XM_011539302.1:c.2029G>T
|
XP_011537604.1:p.Glu677Ter
|
|
XM_011539308.1:c.*35G>T
|
XP_011537610.1:n.*35G>T
|
|
XM_011539309.1:c.1525G>T
|
XP_011537611.1:p.Glu509Ter
|
|
NM_080722.4:c.2956G>T
MANE Select
|
NP_542453.2:p.Glu986Ter
|
|
NM_139155.3:c.2965G>T
|
NP_631894.2:p.Glu989Ter
|
|
XM_011539300.2:c.2455G>T
|
XP_011537602.1:p.Glu819Ter
|
|
XM_011539301.2:c.2029G>T
|
XP_011537603.1:p.Glu677Ter
|
|
XM_011539302.2:c.2029G>T
|
XP_011537604.1:p.Glu677Ter
|
|
XM_011539308.2:c.*35G>T
|
XP_011537610.1:n.*35G>T
|
|