ENST00000498907.3:c.391T>C
MANE Select
|
ENSP00000427514.1:p.Tyr131His
|
|
ENST00000498907.2:c.391T>C
|
ENSP00000427514.1:p.Tyr131His
|
|
NM_001285829.1:c.34T>C
|
NP_001272758.1:p.Tyr12His
|
|
NM_001287424.1:c.496T>C
|
NP_001274353.1:p.Tyr166His
|
|
NM_001287435.1:c.349T>C
|
NP_001274364.1:p.Tyr117His
|
|
NM_004364.4:c.391T>C
|
NP_004355.2:p.Tyr131His
|
|
NM_001287424.2:c.496T>C
|
NP_001274353.1:p.Tyr166His
|
|
NM_004364.5:c.391T>C
MANE Select
|
NP_004355.2:p.Tyr131His
|
|
NM_001285829.2:c.34T>C
|
NP_001272758.1:p.Tyr12His
|
|
NM_001287435.2:c.349T>C
|
NP_001274364.1:p.Tyr117His
|
|