ENST00000367615.9:c.520A>G
MANE Select
|
ENSP00000356587.4:p.Ile174Val
|
|
ENST00000367615.8:c.520A>G
|
ENSP00000356587.4:p.Ile174Val
|
|
ENST00000367616.4:c.520A>G
|
ENSP00000356588.4:p.Ile174Val
|
|
NM_001297575.1:c.520A>G
|
NP_001284504.1:p.Ile174Val
|
|
NM_014625.3:c.520A>G , LRG_887t1:c.520A>G
|
NP_055440.1:p.Ile174Val
|
|
XM_005245483.2:c.343A>G
|
XP_005245540.1:p.Ile115Val
|
|
XM_006711529.2:c.520A>G
|
XP_006711592.1:p.Ile174Val
|
|
XM_005245483.3:c.343A>G
|
XP_005245540.1:p.Ile115Val
|
|
XM_017002298.1:c.447A>G
|
XP_016857787.1:p.Arg149=
|
|
XM_017002299.1:c.520A>G
|
XP_016857788.1:p.Ile174Val
|
|
NM_001297575.2:c.520A>G
|
NP_001284504.1:p.Ile174Val
|
|
NM_014625.4:c.520A>G
MANE Select
|
NP_055440.1:p.Ile174Val
|
|