ENST00000262367.10:c.4517T>C
MANE Select
|
ENSP00000262367.5:p.Met1506Thr
|
|
ENST00000262367.9:c.4517T>C
|
ENSP00000262367.5:p.Met1506Thr
|
|
ENST00000382070.7:c.4403T>C
|
ENSP00000371502.3:p.Met1468Thr
|
|
ENST00000570939.2:c.3152T>C
|
ENSP00000461002.2:p.Met1051Thr
|
|
ENST00000571763.5:n.307T>C
|
|
|
ENST00000574740.1:n.338T>C
|
|
|
ENST00000576720.1:n.3340T>C
|
|
|
NM_001079846.1:c.4403T>C
|
NP_001073315.1:p.Met1468Thr
|
|
NM_004380.2:c.4517T>C
|
NP_004371.2:p.Met1506Thr
|
|
XM_005255124.3:c.4472T>C
|
XP_005255181.1:p.Met1491Thr
|
|
XM_005255125.3:c.4100T>C
|
XP_005255182.1:p.Met1367Thr
|
|
XM_006720848.2:c.4256T>C
|
XP_006720911.1:p.Met1419Thr
|
|
XM_011522380.1:c.4463T>C
|
XP_011520682.1:p.Met1488Thr
|
|
XM_011522381.1:c.3764T>C
|
XP_011520683.1:p.Met1255Thr
|
|
XM_005255124.4:c.4472T>C
|
XP_005255181.1:p.Met1491Thr
|
|
XM_005255125.4:c.4100T>C
|
XP_005255182.1:p.Met1367Thr
|
|
XM_006720848.3:c.4256T>C
|
XP_006720911.1:p.Met1419Thr
|
|
XM_011522381.2:c.3764T>C
|
XP_011520683.1:p.Met1255Thr
|
|
XM_017022944.1:c.4511T>C
|
XP_016878433.1:p.Met1504Thr
|
|
NM_004380.3:c.4517T>C
MANE Select
|
NP_004371.2:p.Met1506Thr
|
|