ENST00000262367.10:c.4515G>A
MANE Select
|
ENSP00000262367.5:p.Lys1505=
|
|
ENST00000262367.9:c.4515G>A
|
ENSP00000262367.5:p.Lys1505=
|
|
ENST00000382070.7:c.4401G>A
|
ENSP00000371502.3:p.Lys1467=
|
|
ENST00000570939.2:c.3150G>A
|
ENSP00000461002.2:p.Lys1050=
|
|
ENST00000571763.5:n.305G>A
|
|
|
ENST00000574740.1:n.336G>A
|
|
|
ENST00000576720.1:n.3338G>A
|
|
|
NM_001079846.1:c.4401G>A
|
NP_001073315.1:p.Lys1467=
|
|
NM_004380.2:c.4515G>A
|
NP_004371.2:p.Lys1505=
|
|
XM_005255124.3:c.4470G>A
|
XP_005255181.1:p.Lys1490=
|
|
XM_005255125.3:c.4098G>A
|
XP_005255182.1:p.Lys1366=
|
|
XM_006720848.2:c.4254G>A
|
XP_006720911.1:p.Lys1418=
|
|
XM_011522380.1:c.4461G>A
|
XP_011520682.1:p.Lys1487=
|
|
XM_011522381.1:c.3762G>A
|
XP_011520683.1:p.Lys1254=
|
|
XM_005255124.4:c.4470G>A
|
XP_005255181.1:p.Lys1490=
|
|
XM_005255125.4:c.4098G>A
|
XP_005255182.1:p.Lys1366=
|
|
XM_006720848.3:c.4254G>A
|
XP_006720911.1:p.Lys1418=
|
|
XM_011522381.2:c.3762G>A
|
XP_011520683.1:p.Lys1254=
|
|
XM_017022944.1:c.4509G>A
|
XP_016878433.1:p.Lys1503=
|
|
NM_004380.3:c.4515G>A
MANE Select
|
NP_004371.2:p.Lys1505=
|
|