ENST00000262367.10:c.5577G>T
MANE Select
|
ENSP00000262367.5:p.Leu1859=
|
|
ENST00000262367.9:c.5577G>T
|
ENSP00000262367.5:p.Leu1859=
|
|
ENST00000382070.7:c.5463G>T
|
ENSP00000371502.3:p.Leu1821=
|
|
NM_001079846.1:c.5463G>T
|
NP_001073315.1:p.Leu1821=
|
|
NM_004380.2:c.5577G>T
|
NP_004371.2:p.Leu1859=
|
|
XM_005255124.3:c.5532G>T
|
XP_005255181.1:p.Leu1844=
|
|
XM_005255125.3:c.5160G>T
|
XP_005255182.1:p.Leu1720=
|
|
XM_006720848.2:c.5316G>T
|
XP_006720911.1:p.Leu1772=
|
|
XM_011522380.1:c.5523G>T
|
XP_011520682.1:p.Leu1841=
|
|
XM_011522381.1:c.4824G>T
|
XP_011520683.1:p.Leu1608=
|
|
XM_005255124.4:c.5532G>T
|
XP_005255181.1:p.Leu1844=
|
|
XM_005255125.4:c.5160G>T
|
XP_005255182.1:p.Leu1720=
|
|
XM_006720848.3:c.5316G>T
|
XP_006720911.1:p.Leu1772=
|
|
XM_011522381.2:c.4824G>T
|
XP_011520683.1:p.Leu1608=
|
|
XM_017022944.1:c.5571G>T
|
XP_016878433.1:p.Leu1857=
|
|
NM_004380.3:c.5577G>T
MANE Select
|
NP_004371.2:p.Leu1859=
|
|