ENST00000262367.10:c.848C=
MANE Select
|
ENSP00000262367.5:p.Ala283=
|
|
ENST00000635899.1:n.90C=
|
|
|
ENST00000262367.9:c.848C=
|
ENSP00000262367.5:p.Ala283=
|
|
ENST00000382070.7:c.848C=
|
ENSP00000371502.3:p.Ala283=
|
|
NM_001079846.1:c.848C=
|
NP_001073315.1:p.Ala283=
|
|
NM_004380.2:c.848C=
|
NP_004371.2:p.Ala283=
|
|
XM_005255124.3:c.848C=
|
XP_005255181.1:p.Ala283=
|
|
XM_005255125.3:c.848C=
|
XP_005255182.1:p.Ala283=
|
|
XM_006720848.2:c.848C=
|
XP_006720911.1:p.Ala283=
|
|
XM_011522380.1:c.794C=
|
XP_011520682.1:p.Ala265=
|
|
XM_011522381.1:c.95C=
|
XP_011520683.1:p.Ala32=
|
|
XM_011522382.1:c.848C=
|
XP_011520684.1:p.Ala283=
|
|
XM_005255124.4:c.848C=
|
XP_005255181.1:p.Ala283=
|
|
XM_005255125.4:c.848C=
|
XP_005255182.1:p.Ala283=
|
|
XM_006720848.3:c.848C=
|
XP_006720911.1:p.Ala283=
|
|
XM_011522381.2:c.95C=
|
XP_011520683.1:p.Ala32=
|
|
XM_011522382.3:c.848C=
|
XP_011520684.1:p.Ala283=
|
|
XM_017022944.1:c.848C=
|
XP_016878433.1:p.Ala283=
|
|
NM_004380.3:c.848C=
MANE Select
|
NP_004371.2:p.Ala283=
|
|