ENST00000209873.9:c.*7A>G
MANE Select
|
ENSP00000209873.4:n.*7A>G
|
|
ENST00000547757.2:c.*566A>G
|
ENSP00000448020.2:n.*566A>G
|
|
ENST00000548931.6:c.1083A>G
|
ENSP00000457518.1:n.1083A>G
|
|
ENST00000549450.6:n.1582A>G
|
|
|
ENST00000209873.8:c.*7A>G
|
ENSP00000209873.4:n.*7A>G
|
|
ENST00000394384.7:c.*7A>G
|
ENSP00000377908.3:n.*7A>G
|
|
ENST00000550286.5:c.*7A>G
|
ENSP00000446885.1:n.*7A>G
|
|
ENST00000552876.5:n.1991A>G
|
|
|
NM_001173466.1:c.*7A>G
|
NP_001166937.1:n.*7A>G
|
|
NM_015665.5:c.*7A>G
|
NP_056480.1:n.*7A>G
|
|
XM_006719617.2:c.*7A>G
|
XP_006719680.1:n.*7A>G
|
|
XM_011538777.1:c.*7A>G
|
XP_011537079.1:n.*7A>G
|
|
XM_011538778.1:c.*7A>G
|
XP_011537080.1:n.*7A>G
|
|
XM_011538779.1:c.*7A>G
|
XP_011537081.1:n.*7A>G
|
|
XM_011538780.1:c.*7A>G
|
XP_011537082.1:n.*7A>G
|
|
XM_011538781.1:c.*7A>G
|
XP_011537083.1:n.*7A>G
|
|
XM_011538778.2:c.*7A>G
|
XP_011537080.1:n.*7A>G
|
|
XM_011538780.2:c.*7A>G
|
XP_011537082.1:n.*7A>G
|
|
NM_015665.6:c.*7A>G
MANE Select
|
NP_056480.1:n.*7A>G
|
|
NM_001173466.2:c.*7A>G
|
NP_001166937.1:n.*7A>G
|
|