ENST00000262367.10:c.4522G>T
MANE Select
|
ENSP00000262367.5:p.Asp1508Tyr
|
|
ENST00000262367.9:c.4522G>T
|
ENSP00000262367.5:p.Asp1508Tyr
|
|
ENST00000382070.7:c.4408G>T
|
ENSP00000371502.3:p.Asp1470Tyr
|
|
ENST00000570939.2:c.3157G>T
|
ENSP00000461002.2:p.Asp1053Tyr
|
|
ENST00000571763.5:n.312G>T
|
|
|
ENST00000574740.1:n.343G>T
|
|
|
ENST00000576720.1:n.3345G>T
|
|
|
NM_001079846.1:c.4408G>T
|
NP_001073315.1:p.Asp1470Tyr
|
|
NM_004380.2:c.4522G>T
|
NP_004371.2:p.Asp1508Tyr
|
|
XM_005255124.3:c.4477G>T
|
XP_005255181.1:p.Asp1493Tyr
|
|
XM_005255125.3:c.4105G>T
|
XP_005255182.1:p.Asp1369Tyr
|
|
XM_006720848.2:c.4261G>T
|
XP_006720911.1:p.Asp1421Tyr
|
|
XM_011522380.1:c.4468G>T
|
XP_011520682.1:p.Asp1490Tyr
|
|
XM_011522381.1:c.3769G>T
|
XP_011520683.1:p.Asp1257Tyr
|
|
XM_005255124.4:c.4477G>T
|
XP_005255181.1:p.Asp1493Tyr
|
|
XM_005255125.4:c.4105G>T
|
XP_005255182.1:p.Asp1369Tyr
|
|
XM_006720848.3:c.4261G>T
|
XP_006720911.1:p.Asp1421Tyr
|
|
XM_011522381.2:c.3769G>T
|
XP_011520683.1:p.Asp1257Tyr
|
|
XM_017022944.1:c.4516G>T
|
XP_016878433.1:p.Asp1506Tyr
|
|
NM_004380.3:c.4522G>T
MANE Select
|
NP_004371.2:p.Asp1508Tyr
|
|