ENST00000262367.10:c.7101A>T
MANE Select
|
ENSP00000262367.5:p.Ile2367=
|
|
ENST00000262367.9:c.7101A>T
|
ENSP00000262367.5:p.Ile2367=
|
|
ENST00000382070.7:c.6987A>T
|
ENSP00000371502.3:p.Ile2329=
|
|
NM_001079846.1:c.6987A>T
|
NP_001073315.1:p.Ile2329=
|
|
NM_004380.2:c.7101A>T
|
NP_004371.2:p.Ile2367=
|
|
XM_005255124.3:c.7056A>T
|
XP_005255181.1:p.Ile2352=
|
|
XM_005255125.3:c.6684A>T
|
XP_005255182.1:p.Ile2228=
|
|
XM_006720848.2:c.6840A>T
|
XP_006720911.1:p.Ile2280=
|
|
XM_011522380.1:c.7047A>T
|
XP_011520682.1:p.Ile2349=
|
|
XM_011522381.1:c.6348A>T
|
XP_011520683.1:p.Ile2116=
|
|
XM_005255124.4:c.7056A>T
|
XP_005255181.1:p.Ile2352=
|
|
XM_005255125.4:c.6684A>T
|
XP_005255182.1:p.Ile2228=
|
|
XM_006720848.3:c.6840A>T
|
XP_006720911.1:p.Ile2280=
|
|
XM_011522381.2:c.6348A>T
|
XP_011520683.1:p.Ile2116=
|
|
XM_017022944.1:c.7095A>T
|
XP_016878433.1:p.Ile2365=
|
|
NM_004380.3:c.7101A>T
MANE Select
|
NP_004371.2:p.Ile2367=
|
|