ENST00000262367.10:c.3519A>G
MANE Select
|
ENSP00000262367.5:p.Arg1173=
|
|
ENST00000262367.9:c.3519A>G
|
ENSP00000262367.5:p.Arg1173=
|
|
ENST00000382070.7:c.3405A>G
|
ENSP00000371502.3:p.Arg1135=
|
|
ENST00000570939.2:c.2124A>G
|
ENSP00000461002.2:p.Arg708=
|
|
NM_001079846.1:c.3405A>G
|
NP_001073315.1:p.Arg1135=
|
|
NM_004380.2:c.3519A>G
|
NP_004371.2:p.Arg1173=
|
|
XM_005255124.3:c.3474A>G
|
XP_005255181.1:p.Arg1158=
|
|
XM_005255125.3:c.3102A>G
|
XP_005255182.1:p.Arg1034=
|
|
XM_006720848.2:c.3519A>G
|
XP_006720911.1:p.Arg1173=
|
|
XM_011522380.1:c.3465A>G
|
XP_011520682.1:p.Arg1155=
|
|
XM_011522381.1:c.2766A>G
|
XP_011520683.1:p.Arg922=
|
|
XM_011522382.1:c.3519A>G
|
XP_011520684.1:p.Arg1173=
|
|
XM_005255124.4:c.3474A>G
|
XP_005255181.1:p.Arg1158=
|
|
XM_005255125.4:c.3102A>G
|
XP_005255182.1:p.Arg1034=
|
|
XM_006720848.3:c.3519A>G
|
XP_006720911.1:p.Arg1173=
|
|
XM_011522381.2:c.2766A>G
|
XP_011520683.1:p.Arg922=
|
|
XM_011522382.3:c.3519A>G
|
XP_011520684.1:p.Arg1173=
|
|
XM_017022944.1:c.3513A>G
|
XP_016878433.1:p.Arg1171=
|
|
NM_004380.3:c.3519A>G
MANE Select
|
NP_004371.2:p.Arg1173=
|
|