ENST00000262367.10:c.4481C>A
MANE Select
|
ENSP00000262367.5:p.Pro1494His
|
|
ENST00000262367.9:c.4481C>A
|
ENSP00000262367.5:p.Pro1494His
|
|
ENST00000382070.7:c.4367C>A
|
ENSP00000371502.3:p.Pro1456His
|
|
ENST00000570939.2:c.3116C>A
|
ENSP00000461002.2:p.Pro1039His
|
|
ENST00000571763.5:n.271C>A
|
|
|
ENST00000574740.1:n.302C>A
|
|
|
ENST00000576720.1:n.3304C>A
|
|
|
NM_001079846.1:c.4367C>A
|
NP_001073315.1:p.Pro1456His
|
|
NM_004380.2:c.4481C>A
|
NP_004371.2:p.Pro1494His
|
|
XM_005255124.3:c.4436C>A
|
XP_005255181.1:p.Pro1479His
|
|
XM_005255125.3:c.4064C>A
|
XP_005255182.1:p.Pro1355His
|
|
XM_006720848.2:c.4220C>A
|
XP_006720911.1:p.Pro1407His
|
|
XM_011522380.1:c.4427C>A
|
XP_011520682.1:p.Pro1476His
|
|
XM_011522381.1:c.3728C>A
|
XP_011520683.1:p.Pro1243His
|
|
XM_005255124.4:c.4436C>A
|
XP_005255181.1:p.Pro1479His
|
|
XM_005255125.4:c.4064C>A
|
XP_005255182.1:p.Pro1355His
|
|
XM_006720848.3:c.4220C>A
|
XP_006720911.1:p.Pro1407His
|
|
XM_011522381.2:c.3728C>A
|
XP_011520683.1:p.Pro1243His
|
|
XM_017022944.1:c.4475C>A
|
XP_016878433.1:p.Pro1492His
|
|
NM_004380.3:c.4481C>A
MANE Select
|
NP_004371.2:p.Pro1494His
|
|