ENST00000262367.10:c.6959T>C
MANE Select
|
ENSP00000262367.5:p.Met2320Thr
|
|
ENST00000262367.9:c.6959T>C
|
ENSP00000262367.5:p.Met2320Thr
|
|
ENST00000382070.7:c.6845T>C
|
ENSP00000371502.3:p.Met2282Thr
|
|
NM_001079846.1:c.6845T>C
|
NP_001073315.1:p.Met2282Thr
|
|
NM_004380.2:c.6959T>C
|
NP_004371.2:p.Met2320Thr
|
|
XM_005255124.3:c.6914T>C
|
XP_005255181.1:p.Met2305Thr
|
|
XM_005255125.3:c.6542T>C
|
XP_005255182.1:p.Met2181Thr
|
|
XM_006720848.2:c.6698T>C
|
XP_006720911.1:p.Met2233Thr
|
|
XM_011522380.1:c.6905T>C
|
XP_011520682.1:p.Met2302Thr
|
|
XM_011522381.1:c.6206T>C
|
XP_011520683.1:p.Met2069Thr
|
|
XM_005255124.4:c.6914T>C
|
XP_005255181.1:p.Met2305Thr
|
|
XM_005255125.4:c.6542T>C
|
XP_005255182.1:p.Met2181Thr
|
|
XM_006720848.3:c.6698T>C
|
XP_006720911.1:p.Met2233Thr
|
|
XM_011522381.2:c.6206T>C
|
XP_011520683.1:p.Met2069Thr
|
|
XM_017022944.1:c.6953T>C
|
XP_016878433.1:p.Met2318Thr
|
|
NM_004380.3:c.6959T>C
MANE Select
|
NP_004371.2:p.Met2320Thr
|
|