ENST00000262367.10:c.6999G>A
MANE Select
|
ENSP00000262367.5:p.Gln2333=
|
|
ENST00000262367.9:c.6999G>A
|
ENSP00000262367.5:p.Gln2333=
|
|
ENST00000382070.7:c.6885G>A
|
ENSP00000371502.3:p.Gln2295=
|
|
NM_001079846.1:c.6885G>A
|
NP_001073315.1:p.Gln2295=
|
|
NM_004380.2:c.6999G>A
|
NP_004371.2:p.Gln2333=
|
|
XM_005255124.3:c.6954G>A
|
XP_005255181.1:p.Gln2318=
|
|
XM_005255125.3:c.6582G>A
|
XP_005255182.1:p.Gln2194=
|
|
XM_006720848.2:c.6738G>A
|
XP_006720911.1:p.Gln2246=
|
|
XM_011522380.1:c.6945G>A
|
XP_011520682.1:p.Gln2315=
|
|
XM_011522381.1:c.6246G>A
|
XP_011520683.1:p.Gln2082=
|
|
XM_005255124.4:c.6954G>A
|
XP_005255181.1:p.Gln2318=
|
|
XM_005255125.4:c.6582G>A
|
XP_005255182.1:p.Gln2194=
|
|
XM_006720848.3:c.6738G>A
|
XP_006720911.1:p.Gln2246=
|
|
XM_011522381.2:c.6246G>A
|
XP_011520683.1:p.Gln2082=
|
|
XM_017022944.1:c.6993G>A
|
XP_016878433.1:p.Gln2331=
|
|
NM_004380.3:c.6999G>A
MANE Select
|
NP_004371.2:p.Gln2333=
|
|