ENST00000262367.10:c.3331T>A
MANE Select
|
ENSP00000262367.5:p.Phe1111Ile
|
|
ENST00000262367.9:c.3331T>A
|
ENSP00000262367.5:p.Phe1111Ile
|
|
ENST00000382070.7:c.3217T>A
|
ENSP00000371502.3:p.Phe1073Ile
|
|
ENST00000570939.2:c.1936T>A
|
ENSP00000461002.2:p.Phe646Ile
|
|
NM_001079846.1:c.3217T>A
|
NP_001073315.1:p.Phe1073Ile
|
|
NM_004380.2:c.3331T>A
|
NP_004371.2:p.Phe1111Ile
|
|
XM_005255124.3:c.3286T>A
|
XP_005255181.1:p.Phe1096Ile
|
|
XM_005255125.3:c.2914T>A
|
XP_005255182.1:p.Phe972Ile
|
|
XM_006720848.2:c.3331T>A
|
XP_006720911.1:p.Phe1111Ile
|
|
XM_011522380.1:c.3277T>A
|
XP_011520682.1:p.Phe1093Ile
|
|
XM_011522381.1:c.2578T>A
|
XP_011520683.1:p.Phe860Ile
|
|
XM_011522382.1:c.3331T>A
|
XP_011520684.1:p.Phe1111Ile
|
|
XM_005255124.4:c.3286T>A
|
XP_005255181.1:p.Phe1096Ile
|
|
XM_005255125.4:c.2914T>A
|
XP_005255182.1:p.Phe972Ile
|
|
XM_006720848.3:c.3331T>A
|
XP_006720911.1:p.Phe1111Ile
|
|
XM_011522381.2:c.2578T>A
|
XP_011520683.1:p.Phe860Ile
|
|
XM_011522382.3:c.3331T>A
|
XP_011520684.1:p.Phe1111Ile
|
|
XM_017022944.1:c.3325T>A
|
XP_016878433.1:p.Phe1109Ile
|
|
NM_004380.3:c.3331T>A
MANE Select
|
NP_004371.2:p.Phe1111Ile
|
|