ENST00000262367.10:c.6978G>A
MANE Select
|
ENSP00000262367.5:p.Gln2326=
|
|
ENST00000262367.9:c.6978G>A
|
ENSP00000262367.5:p.Gln2326=
|
|
ENST00000382070.7:c.6864G>A
|
ENSP00000371502.3:p.Gln2288=
|
|
NM_001079846.1:c.6864G>A
|
NP_001073315.1:p.Gln2288=
|
|
NM_004380.2:c.6978G>A
|
NP_004371.2:p.Gln2326=
|
|
XM_005255124.3:c.6933G>A
|
XP_005255181.1:p.Gln2311=
|
|
XM_005255125.3:c.6561G>A
|
XP_005255182.1:p.Gln2187=
|
|
XM_006720848.2:c.6717G>A
|
XP_006720911.1:p.Gln2239=
|
|
XM_011522380.1:c.6924G>A
|
XP_011520682.1:p.Gln2308=
|
|
XM_011522381.1:c.6225G>A
|
XP_011520683.1:p.Gln2075=
|
|
XM_005255124.4:c.6933G>A
|
XP_005255181.1:p.Gln2311=
|
|
XM_005255125.4:c.6561G>A
|
XP_005255182.1:p.Gln2187=
|
|
XM_006720848.3:c.6717G>A
|
XP_006720911.1:p.Gln2239=
|
|
XM_011522381.2:c.6225G>A
|
XP_011520683.1:p.Gln2075=
|
|
XM_017022944.1:c.6972G>A
|
XP_016878433.1:p.Gln2324=
|
|
NM_004380.3:c.6978G>A
MANE Select
|
NP_004371.2:p.Gln2326=
|
|