ENST00000682617.1:c.*318A>T
|
ENSP00000507912.1:n.*318A>T
|
|
ENST00000683962.1:c.*2763A>T
|
ENSP00000506854.1:n.*2763A>T
|
|
ENST00000311895.8:c.*318A>T
MANE Select
|
ENSP00000310520.7:n.*318A>T
|
|
ENST00000311895.7:c.*318A>T
|
ENSP00000310520.7:n.*318A>T
|
|
NM_005236.2:c.*318A>T , LRG_463t1:c.*318A>T
|
NP_005227.1:n.*318A>T
|
|
XM_011522424.1:c.*318A>T
|
XP_011520726.1:n.*318A>T
|
|
XM_011522425.1:c.*318A>T
|
XP_011520727.1:n.*318A>T
|
|
XM_011522426.1:c.*318A>T
|
XP_011520728.1:n.*318A>T
|
|
XM_011522427.1:c.*318A>T
|
XP_011520729.1:n.*318A>T
|
|
XR_932805.1:n.3074-48A>T
|
|
|
XM_011522424.3:c.*318A>T
|
XP_011520726.1:n.*318A>T
|
|
XM_017023043.2:c.*318A>T
|
XP_016878532.1:n.*318A>T
|
|
NM_005236.3:c.*318A>T
MANE Select
|
NP_005227.1:n.*318A>T
|
|