ENST00000334785.12:c.1538T>C
MANE Select
|
ENSP00000333938.7:p.Met513Thr
|
|
ENST00000330010.12:c.1346T>C
|
ENSP00000327363.8:p.Met449Thr
|
|
ENST00000334785.11:c.1538T>C
|
ENSP00000333938.7:p.Met513Thr
|
|
ENST00000342754.5:c.1237T>C
|
|
|
ENST00000470735.1:n.377T>C
|
|
|
ENST00000480732.2:n.1112T>C
|
|
|
NM_001172309.1:c.1346T>C
|
NP_001165780.1:p.Met449Thr
|
|
NM_144573.3:c.1538T>C , LRG_442t1:c.1538T>C
|
NP_653174.3:p.Met513Thr
|
|
XM_005271322.2:c.1538T>C
|
XP_005271379.1:p.Met513Thr
|
|
XM_005271323.2:c.1496T>C
|
XP_005271380.1:p.Met499Thr
|
|
XM_005271324.3:c.1346T>C
|
XP_005271381.1:p.Met449Thr
|
|
XM_005271325.2:c.1316T>C
|
XP_005271382.1:p.Met439Thr
|
|
XM_005271326.2:c.1304T>C
|
XP_005271383.1:p.Met435Thr
|
|
XM_005271327.2:c.1121T>C
|
XP_005271384.1:p.Met374Thr
|
|
XM_005271322.4:c.1538T>C
|
XP_005271379.1:p.Met513Thr
|
|
XM_005271323.4:c.1496T>C
|
XP_005271380.1:p.Met499Thr
|
|
XM_005271324.5:c.1346T>C
|
XP_005271381.1:p.Met449Thr
|
|
XM_005271325.4:c.1316T>C
|
XP_005271382.1:p.Met439Thr
|
|
XM_005271326.4:c.1304T>C
|
XP_005271383.1:p.Met435Thr
|
|
XM_005271327.4:c.1121T>C
|
XP_005271384.1:p.Met374Thr
|
|
NM_001172309.2:c.1346T>C
|
NP_001165780.1:p.Met449Thr
|
|
NM_144573.4:c.1538T>C
MANE Select
|
NP_653174.3:p.Met513Thr
|
|