ENST00000262367.10:c.4491A>G
MANE Select
|
ENSP00000262367.5:p.Lys1497=
|
|
ENST00000262367.9:c.4491A>G
|
ENSP00000262367.5:p.Lys1497=
|
|
ENST00000382070.7:c.4377A>G
|
ENSP00000371502.3:p.Lys1459=
|
|
ENST00000570939.2:c.3126A>G
|
ENSP00000461002.2:p.Lys1042=
|
|
ENST00000571763.5:n.281A>G
|
|
|
ENST00000574740.1:n.312A>G
|
|
|
ENST00000576720.1:n.3314A>G
|
|
|
NM_001079846.1:c.4377A>G
|
NP_001073315.1:p.Lys1459=
|
|
NM_004380.2:c.4491A>G
|
NP_004371.2:p.Lys1497=
|
|
XM_005255124.3:c.4446A>G
|
XP_005255181.1:p.Lys1482=
|
|
XM_005255125.3:c.4074A>G
|
XP_005255182.1:p.Lys1358=
|
|
XM_006720848.2:c.4230A>G
|
XP_006720911.1:p.Lys1410=
|
|
XM_011522380.1:c.4437A>G
|
XP_011520682.1:p.Lys1479=
|
|
XM_011522381.1:c.3738A>G
|
XP_011520683.1:p.Lys1246=
|
|
XM_005255124.4:c.4446A>G
|
XP_005255181.1:p.Lys1482=
|
|
XM_005255125.4:c.4074A>G
|
XP_005255182.1:p.Lys1358=
|
|
XM_006720848.3:c.4230A>G
|
XP_006720911.1:p.Lys1410=
|
|
XM_011522381.2:c.3738A>G
|
XP_011520683.1:p.Lys1246=
|
|
XM_017022944.1:c.4485A>G
|
XP_016878433.1:p.Lys1495=
|
|
NM_004380.3:c.4491A>G
MANE Select
|
NP_004371.2:p.Lys1497=
|
|