ENST00000262367.10:c.6962T>A
MANE Select
|
ENSP00000262367.5:p.Leu2321His
|
|
ENST00000262367.9:c.6962T>A
|
ENSP00000262367.5:p.Leu2321His
|
|
ENST00000382070.7:c.6848T>A
|
ENSP00000371502.3:p.Leu2283His
|
|
NM_001079846.1:c.6848T>A
|
NP_001073315.1:p.Leu2283His
|
|
NM_004380.2:c.6962T>A
|
NP_004371.2:p.Leu2321His
|
|
XM_005255124.3:c.6917T>A
|
XP_005255181.1:p.Leu2306His
|
|
XM_005255125.3:c.6545T>A
|
XP_005255182.1:p.Leu2182His
|
|
XM_006720848.2:c.6701T>A
|
XP_006720911.1:p.Leu2234His
|
|
XM_011522380.1:c.6908T>A
|
XP_011520682.1:p.Leu2303His
|
|
XM_011522381.1:c.6209T>A
|
XP_011520683.1:p.Leu2070His
|
|
XM_005255124.4:c.6917T>A
|
XP_005255181.1:p.Leu2306His
|
|
XM_005255125.4:c.6545T>A
|
XP_005255182.1:p.Leu2182His
|
|
XM_006720848.3:c.6701T>A
|
XP_006720911.1:p.Leu2234His
|
|
XM_011522381.2:c.6209T>A
|
XP_011520683.1:p.Leu2070His
|
|
XM_017022944.1:c.6956T>A
|
XP_016878433.1:p.Leu2319His
|
|
NM_004380.3:c.6962T>A
MANE Select
|
NP_004371.2:p.Leu2321His
|
|