ENST00000393067.8:c.*2000G>A
MANE Select
|
ENSP00000376786.3:n.*2000G>A
|
|
ENST00000393067.7:c.*2000G>A
|
ENSP00000376786.3:n.*2000G>A
|
|
NM_006235.2:c.*2000G>A
|
NP_006226.2:n.*2000G>A
|
|
XM_005271593.1:c.*2000G>A
|
XP_005271650.1:n.*2000G>A
|
|
XM_005271594.3:c.*2000G>A
|
XP_005271651.1:n.*2000G>A
|
|
XM_006718859.1:c.*2000G>A
|
XP_006718922.1:n.*2000G>A
|
|
XM_005271593.2:c.*2000G>A
|
XP_005271650.1:n.*2000G>A
|
|
XM_006718860.4:c.*4155G>A
|
XP_006718923.1:n.*4155G>A
|
|
XM_017017932.1:c.*4155G>A
|
XP_016873421.1:n.*4155G>A
|
|
NM_006235.3:c.*2000G>A
MANE Select
|
NP_006226.2:n.*2000G>A
|
|