ENST00000262367.10:c.7257G>T
MANE Select
|
ENSP00000262367.5:p.Ala2419=
|
|
ENST00000262367.9:c.7257G>T
|
ENSP00000262367.5:p.Ala2419=
|
|
ENST00000382070.7:c.7143G>T
|
ENSP00000371502.3:p.Ala2381=
|
|
NM_001079846.1:c.7143G>T
|
NP_001073315.1:p.Ala2381=
|
|
NM_004380.2:c.7257G>T
|
NP_004371.2:p.Ala2419=
|
|
XM_005255124.3:c.7212G>T
|
XP_005255181.1:p.Ala2404=
|
|
XM_005255125.3:c.6840G>T
|
XP_005255182.1:p.Ala2280=
|
|
XM_006720848.2:c.6996G>T
|
XP_006720911.1:p.Ala2332=
|
|
XM_011522380.1:c.7203G>T
|
XP_011520682.1:p.Ala2401=
|
|
XM_011522381.1:c.6504G>T
|
XP_011520683.1:p.Ala2168=
|
|
XM_005255124.4:c.7212G>T
|
XP_005255181.1:p.Ala2404=
|
|
XM_005255125.4:c.6840G>T
|
XP_005255182.1:p.Ala2280=
|
|
XM_006720848.3:c.6996G>T
|
XP_006720911.1:p.Ala2332=
|
|
XM_011522381.2:c.6504G>T
|
XP_011520683.1:p.Ala2168=
|
|
XM_017022944.1:c.7251G>T
|
XP_016878433.1:p.Ala2417=
|
|
NM_004380.3:c.7257G>T
MANE Select
|
NP_004371.2:p.Ala2419=
|
|