ENST00000262367.10:c.3517C>G
MANE Select
|
ENSP00000262367.5:p.Arg1173Gly
|
|
ENST00000262367.9:c.3517C>G
|
ENSP00000262367.5:p.Arg1173Gly
|
|
ENST00000382070.7:c.3403C>G
|
ENSP00000371502.3:p.Arg1135Gly
|
|
ENST00000570939.2:c.2122C>G
|
ENSP00000461002.2:p.Arg708Gly
|
|
NM_001079846.1:c.3403C>G
|
NP_001073315.1:p.Arg1135Gly
|
|
NM_004380.2:c.3517C>G
|
NP_004371.2:p.Arg1173Gly
|
|
XM_005255124.3:c.3472C>G
|
XP_005255181.1:p.Arg1158Gly
|
|
XM_005255125.3:c.3100C>G
|
XP_005255182.1:p.Arg1034Gly
|
|
XM_006720848.2:c.3517C>G
|
XP_006720911.1:p.Arg1173Gly
|
|
XM_011522380.1:c.3463C>G
|
XP_011520682.1:p.Arg1155Gly
|
|
XM_011522381.1:c.2764C>G
|
XP_011520683.1:p.Arg922Gly
|
|
XM_011522382.1:c.3517C>G
|
XP_011520684.1:p.Arg1173Gly
|
|
XM_005255124.4:c.3472C>G
|
XP_005255181.1:p.Arg1158Gly
|
|
XM_005255125.4:c.3100C>G
|
XP_005255182.1:p.Arg1034Gly
|
|
XM_006720848.3:c.3517C>G
|
XP_006720911.1:p.Arg1173Gly
|
|
XM_011522381.2:c.2764C>G
|
XP_011520683.1:p.Arg922Gly
|
|
XM_011522382.3:c.3517C>G
|
XP_011520684.1:p.Arg1173Gly
|
|
XM_017022944.1:c.3511C>G
|
XP_016878433.1:p.Arg1171Gly
|
|
NM_004380.3:c.3517C>G
MANE Select
|
NP_004371.2:p.Arg1173Gly
|
|