ENST00000205402.10:c.1156T>C
MANE Select
|
ENSP00000205402.3:p.Tyr386His
|
|
ENST00000205402.9:c.1156T>C
|
ENSP00000205402.3:p.Tyr386His
|
|
ENST00000415325.5:c.*830T>C
|
ENSP00000402593.1:n.*830T>C
|
|
ENST00000417551.5:c.1156T>C
|
ENSP00000390667.1:p.Tyr386His
|
|
ENST00000437604.6:c.1012T>C
|
ENSP00000387542.2:p.Tyr338His
|
|
ENST00000440410.5:c.1087T>C
|
ENSP00000417016.1:p.Tyr363His
|
|
NM_000108.4:c.1156T>C
|
NP_000099.2:p.Tyr386His
|
|
NM_001289750.1:c.859T>C
|
NP_001276679.1:p.Tyr287His
|
|
NM_001289751.1:c.1087T>C
|
NP_001276680.1:p.Tyr363His
|
|
NM_001289752.1:c.1012T>C
|
NP_001276681.1:p.Tyr338His
|
|
NM_000108.5:c.1156T>C
MANE Select
|
NP_000099.2:p.Tyr386His
|
|