ENST00000262367.10:c.5474T>A
MANE Select
|
ENSP00000262367.5:p.Leu1825His
|
|
ENST00000262367.9:c.5474T>A
|
ENSP00000262367.5:p.Leu1825His
|
|
ENST00000382070.7:c.5360T>A
|
ENSP00000371502.3:p.Leu1787His
|
|
NM_001079846.1:c.5360T>A
|
NP_001073315.1:p.Leu1787His
|
|
NM_004380.2:c.5474T>A
|
NP_004371.2:p.Leu1825His
|
|
XM_005255124.3:c.5429T>A
|
XP_005255181.1:p.Leu1810His
|
|
XM_005255125.3:c.5057T>A
|
XP_005255182.1:p.Leu1686His
|
|
XM_006720848.2:c.5213T>A
|
XP_006720911.1:p.Leu1738His
|
|
XM_011522380.1:c.5420T>A
|
XP_011520682.1:p.Leu1807His
|
|
XM_011522381.1:c.4721T>A
|
XP_011520683.1:p.Leu1574His
|
|
XM_005255124.4:c.5429T>A
|
XP_005255181.1:p.Leu1810His
|
|
XM_005255125.4:c.5057T>A
|
XP_005255182.1:p.Leu1686His
|
|
XM_006720848.3:c.5213T>A
|
XP_006720911.1:p.Leu1738His
|
|
XM_011522381.2:c.4721T>A
|
XP_011520683.1:p.Leu1574His
|
|
XM_017022944.1:c.5468T>A
|
XP_016878433.1:p.Leu1823His
|
|
NM_004380.3:c.5474T>A
MANE Select
|
NP_004371.2:p.Leu1825His
|
|