ENST00000262367.10:c.7032G>T
MANE Select
|
ENSP00000262367.5:p.Arg2344=
|
|
ENST00000262367.9:c.7032G>T
|
ENSP00000262367.5:p.Arg2344=
|
|
ENST00000382070.7:c.6918G>T
|
ENSP00000371502.3:p.Arg2306=
|
|
NM_001079846.1:c.6918G>T
|
NP_001073315.1:p.Arg2306=
|
|
NM_004380.2:c.7032G>T
|
NP_004371.2:p.Arg2344=
|
|
XM_005255124.3:c.6987G>T
|
XP_005255181.1:p.Arg2329=
|
|
XM_005255125.3:c.6615G>T
|
XP_005255182.1:p.Arg2205=
|
|
XM_006720848.2:c.6771G>T
|
XP_006720911.1:p.Arg2257=
|
|
XM_011522380.1:c.6978G>T
|
XP_011520682.1:p.Arg2326=
|
|
XM_011522381.1:c.6279G>T
|
XP_011520683.1:p.Arg2093=
|
|
XM_005255124.4:c.6987G>T
|
XP_005255181.1:p.Arg2329=
|
|
XM_005255125.4:c.6615G>T
|
XP_005255182.1:p.Arg2205=
|
|
XM_006720848.3:c.6771G>T
|
XP_006720911.1:p.Arg2257=
|
|
XM_011522381.2:c.6279G>T
|
XP_011520683.1:p.Arg2093=
|
|
XM_017022944.1:c.7026G>T
|
XP_016878433.1:p.Arg2342=
|
|
NM_004380.3:c.7032G>T
MANE Select
|
NP_004371.2:p.Arg2344=
|
|