ENST00000262367.10:c.4403C>G
MANE Select
|
ENSP00000262367.5:p.Thr1468Arg
|
|
ENST00000262367.9:c.4403C>G
|
ENSP00000262367.5:p.Thr1468Arg
|
|
ENST00000382070.7:c.4289C>G
|
ENSP00000371502.3:p.Thr1430Arg
|
|
ENST00000570939.2:c.3038C>G
|
ENSP00000461002.2:p.Thr1013Arg
|
|
ENST00000571763.5:n.193C>G
|
|
|
ENST00000574740.1:n.224C>G
|
|
|
ENST00000576720.1:n.3226C>G
|
|
|
NM_001079846.1:c.4289C>G
|
NP_001073315.1:p.Thr1430Arg
|
|
NM_004380.2:c.4403C>G
|
NP_004371.2:p.Thr1468Arg
|
|
XM_005255124.3:c.4358C>G
|
XP_005255181.1:p.Thr1453Arg
|
|
XM_005255125.3:c.3986C>G
|
XP_005255182.1:p.Thr1329Arg
|
|
XM_006720848.2:c.4142C>G
|
XP_006720911.1:p.Thr1381Arg
|
|
XM_011522380.1:c.4349C>G
|
XP_011520682.1:p.Thr1450Arg
|
|
XM_011522381.1:c.3650C>G
|
XP_011520683.1:p.Thr1217Arg
|
|
XM_005255124.4:c.4358C>G
|
XP_005255181.1:p.Thr1453Arg
|
|
XM_005255125.4:c.3986C>G
|
XP_005255182.1:p.Thr1329Arg
|
|
XM_006720848.3:c.4142C>G
|
XP_006720911.1:p.Thr1381Arg
|
|
XM_011522381.2:c.3650C>G
|
XP_011520683.1:p.Thr1217Arg
|
|
XM_017022944.1:c.4397C>G
|
XP_016878433.1:p.Thr1466Arg
|
|
NM_004380.3:c.4403C>G
MANE Select
|
NP_004371.2:p.Thr1468Arg
|
|