ENST00000290866.10:c.3548T>C
MANE Select
|
ENSP00000290866.4:p.Met1183Thr
|
|
ENST00000290863.10:c.1826T>C
|
ENSP00000290863.6:p.Met609Thr
|
|
ENST00000290866.9:c.3548T>C
|
ENSP00000290866.4:p.Met1183Thr
|
|
ENST00000413513.7:c.1703T>C
|
ENSP00000392247.3:p.Met568Thr
|
|
ENST00000428043.5:c.3548T>C
|
ENSP00000397593.2:p.Met1183Thr
|
|
ENST00000577418.5:n.558T>C
|
|
|
ENST00000577647.2:c.1826T>C
|
ENSP00000464149.1:p.Met609Thr
|
|
ENST00000578839.5:c.*1303T>C
|
ENSP00000462110.2:n.*1303T>C
|
|
ENST00000579314.5:c.*1277T>C
|
ENSP00000462599.1:n.*1277T>C
|
|
ENST00000579409.1:c.235T>C
|
|
|
ENST00000582244.1:n.422T>C
|
|
|
NM_000789.3:c.3548T>C
|
NP_000780.1:p.Met1183Thr
|
|
NM_001178057.1:c.1703T>C
|
NP_001171528.1:p.Met568Thr
|
|
NM_152830.2:c.1826T>C
|
NP_690043.1:p.Met609Thr
|
|
XM_005257110.1:c.2999T>C
|
XP_005257167.1:p.Met1000Thr
|
|
XM_006721737.2:c.1886T>C
|
XP_006721800.2:p.Met629Thr
|
|
XM_006721737.3:c.1886T>C
|
XP_006721800.2:p.Met629Thr
|
|
NM_000789.4:c.3548T>C
MANE Select
|
NP_000780.1:p.Met1183Thr
|
|
NM_001178057.2:c.1703T>C
|
NP_001171528.1:p.Met568Thr
|
|
NM_152830.3:c.1826T>C
|
NP_690043.1:p.Met609Thr
|
|
NM_001382700.1:c.2981T>C
|
NP_001369629.1:p.Met994Thr
|
|
NM_001382701.1:c.2696T>C
|
NP_001369630.1:p.Met899Thr
|
|
NM_001382702.1:c.1163T>C
|
NP_001369631.1:p.Met388Thr
|
|
NR_168483.1:n.1926T>C
|
|
|