ENST00000205402.10:c.712G>C
MANE Select
|
ENSP00000205402.3:p.Asp238His
|
|
ENST00000205402.9:c.712G>C
|
ENSP00000205402.3:p.Asp238His
|
|
ENST00000415325.5:c.*386G>C
|
ENSP00000402593.1:n.*386G>C
|
|
ENST00000417551.5:c.712G>C
|
ENSP00000390667.1:p.Asp238His
|
|
ENST00000437604.6:c.568G>C
|
ENSP00000387542.2:p.Asp190His
|
|
ENST00000440410.5:c.643G>C
|
ENSP00000417016.1:p.Asp215His
|
|
ENST00000451081.5:c.*455G>C
|
ENSP00000388077.1:n.*455G>C
|
|
NM_000108.4:c.712G>C
|
NP_000099.2:p.Asp238His
|
|
NM_001289750.1:c.415G>C
|
NP_001276679.1:p.Asp139His
|
|
NM_001289751.1:c.643G>C
|
NP_001276680.1:p.Asp215His
|
|
NM_001289752.1:c.568G>C
|
NP_001276681.1:p.Asp190His
|
|
NM_000108.5:c.712G>C
MANE Select
|
NP_000099.2:p.Asp238His
|
|