ENST00000262367.10:c.7298A>T
MANE Select
|
ENSP00000262367.5:p.Asp2433Val
|
|
ENST00000262367.9:c.7298A>T
|
ENSP00000262367.5:p.Asp2433Val
|
|
ENST00000382070.7:c.7184A>T
|
ENSP00000371502.3:p.Asp2395Val
|
|
NM_001079846.1:c.7184A>T
|
NP_001073315.1:p.Asp2395Val
|
|
NM_004380.2:c.7298A>T
|
NP_004371.2:p.Asp2433Val
|
|
XM_005255124.3:c.7253A>T
|
XP_005255181.1:p.Asp2418Val
|
|
XM_005255125.3:c.6881A>T
|
XP_005255182.1:p.Asp2294Val
|
|
XM_006720848.2:c.7037A>T
|
XP_006720911.1:p.Asp2346Val
|
|
XM_011522380.1:c.7244A>T
|
XP_011520682.1:p.Asp2415Val
|
|
XM_011522381.1:c.6545A>T
|
XP_011520683.1:p.Asp2182Val
|
|
XM_005255124.4:c.7253A>T
|
XP_005255181.1:p.Asp2418Val
|
|
XM_005255125.4:c.6881A>T
|
XP_005255182.1:p.Asp2294Val
|
|
XM_006720848.3:c.7037A>T
|
XP_006720911.1:p.Asp2346Val
|
|
XM_011522381.2:c.6545A>T
|
XP_011520683.1:p.Asp2182Val
|
|
XM_017022944.1:c.7292A>T
|
XP_016878433.1:p.Asp2431Val
|
|
NM_004380.3:c.7298A>T
MANE Select
|
NP_004371.2:p.Asp2433Val
|
|