ENST00000262367.10:c.4517T>G
MANE Select
|
ENSP00000262367.5:p.Met1506Arg
|
|
ENST00000262367.9:c.4517T>G
|
ENSP00000262367.5:p.Met1506Arg
|
|
ENST00000382070.7:c.4403T>G
|
ENSP00000371502.3:p.Met1468Arg
|
|
ENST00000570939.2:c.3152T>G
|
ENSP00000461002.2:p.Met1051Arg
|
|
ENST00000571763.5:n.307T>G
|
|
|
ENST00000574740.1:n.338T>G
|
|
|
ENST00000576720.1:n.3340T>G
|
|
|
NM_001079846.1:c.4403T>G
|
NP_001073315.1:p.Met1468Arg
|
|
NM_004380.2:c.4517T>G
|
NP_004371.2:p.Met1506Arg
|
|
XM_005255124.3:c.4472T>G
|
XP_005255181.1:p.Met1491Arg
|
|
XM_005255125.3:c.4100T>G
|
XP_005255182.1:p.Met1367Arg
|
|
XM_006720848.2:c.4256T>G
|
XP_006720911.1:p.Met1419Arg
|
|
XM_011522380.1:c.4463T>G
|
XP_011520682.1:p.Met1488Arg
|
|
XM_011522381.1:c.3764T>G
|
XP_011520683.1:p.Met1255Arg
|
|
XM_005255124.4:c.4472T>G
|
XP_005255181.1:p.Met1491Arg
|
|
XM_005255125.4:c.4100T>G
|
XP_005255182.1:p.Met1367Arg
|
|
XM_006720848.3:c.4256T>G
|
XP_006720911.1:p.Met1419Arg
|
|
XM_011522381.2:c.3764T>G
|
XP_011520683.1:p.Met1255Arg
|
|
XM_017022944.1:c.4511T>G
|
XP_016878433.1:p.Met1504Arg
|
|
NM_004380.3:c.4517T>G
MANE Select
|
NP_004371.2:p.Met1506Arg
|
|