ENST00000262367.10:c.4280G>T
MANE Select
|
ENSP00000262367.5:p.Arg1427Met
|
|
ENST00000262367.9:c.4280G>T
|
ENSP00000262367.5:p.Arg1427Met
|
|
ENST00000382070.7:c.4166G>T
|
ENSP00000371502.3:p.Arg1389Met
|
|
ENST00000570939.2:c.2915G>T
|
ENSP00000461002.2:p.Arg972Met
|
|
ENST00000573517.6:c.586G>T
|
|
|
ENST00000574740.1:n.215+821G>T
|
|
|
ENST00000576720.1:n.3217G>T
|
|
|
NM_001079846.1:c.4166G>T
|
NP_001073315.1:p.Arg1389Met
|
|
NM_004380.2:c.4280G>T
|
NP_004371.2:p.Arg1427Met
|
|
XM_005255124.3:c.4235G>T
|
XP_005255181.1:p.Arg1412Met
|
|
XM_005255125.3:c.3863G>T
|
XP_005255182.1:p.Arg1288Met
|
|
XM_006720848.2:c.4133+821G>T
|
XP_006720911.1:n.4133+821G>T
|
|
XM_011522380.1:c.4226G>T
|
XP_011520682.1:p.Arg1409Met
|
|
XM_011522381.1:c.3527G>T
|
XP_011520683.1:p.Arg1176Met
|
|
XM_005255124.4:c.4235G>T
|
XP_005255181.1:p.Arg1412Met
|
|
XM_005255125.4:c.3863G>T
|
XP_005255182.1:p.Arg1288Met
|
|
XM_006720848.3:c.4133+821G>T
|
XP_006720911.1:n.4133+821G>T
|
|
XM_011522381.2:c.3527G>T
|
XP_011520683.1:p.Arg1176Met
|
|
XM_017022944.1:c.4274G>T
|
XP_016878433.1:p.Arg1425Met
|
|
NM_004380.3:c.4280G>T
MANE Select
|
NP_004371.2:p.Arg1427Met
|
|