ENST00000262367.10:c.7097G>A
MANE Select
|
ENSP00000262367.5:p.Arg2366Gln
|
|
ENST00000262367.9:c.7097G>A
|
ENSP00000262367.5:p.Arg2366Gln
|
|
ENST00000382070.7:c.6983G>A
|
ENSP00000371502.3:p.Arg2328Gln
|
|
NM_001079846.1:c.6983G>A
|
NP_001073315.1:p.Arg2328Gln
|
|
NM_004380.2:c.7097G>A
|
NP_004371.2:p.Arg2366Gln
|
|
XM_005255124.3:c.7052G>A
|
XP_005255181.1:p.Arg2351Gln
|
|
XM_005255125.3:c.6680G>A
|
XP_005255182.1:p.Arg2227Gln
|
|
XM_006720848.2:c.6836G>A
|
XP_006720911.1:p.Arg2279Gln
|
|
XM_011522380.1:c.7043G>A
|
XP_011520682.1:p.Arg2348Gln
|
|
XM_011522381.1:c.6344G>A
|
XP_011520683.1:p.Arg2115Gln
|
|
XM_005255124.4:c.7052G>A
|
XP_005255181.1:p.Arg2351Gln
|
|
XM_005255125.4:c.6680G>A
|
XP_005255182.1:p.Arg2227Gln
|
|
XM_006720848.3:c.6836G>A
|
XP_006720911.1:p.Arg2279Gln
|
|
XM_011522381.2:c.6344G>A
|
XP_011520683.1:p.Arg2115Gln
|
|
XM_017022944.1:c.7091G>A
|
XP_016878433.1:p.Arg2364Gln
|
|
NM_004380.3:c.7097G>A
MANE Select
|
NP_004371.2:p.Arg2366Gln
|
|