|
ENST00000526008.6:c.*1938G=
|
ENSP00000513006.1:n.*1938G=
|
|
|
ENST00000696967.1:n.2558G=
|
|
|
|
ENST00000696968.1:n.614G=
|
|
|
|
ENST00000696969.1:n.2338G=
|
|
|
|
ENST00000458235.7:c.*6G=
MANE Select
|
ENSP00000391676.1:n.*6G=
|
|
|
ENST00000458235.5:c.*6G=
|
ENSP00000391676.1:n.*6G=
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|
|
ENST00000527031.5:n.2279-1427G=
|
|
|
|
ENST00000527670.5:c.*6G=
|
ENSP00000432511.1:n.*6G=
|
|
|
NM_000215.3:c.*6G= , LRG_77t1:c.*6G=
|
NP_000206.2:n.*6G=
|
|
|
XM_005259896.2:c.*6G=
|
XP_005259953.1:n.*6G=
|
|
|
XM_006722745.2:c.*6G=
|
XP_006722808.1:n.*6G=
|
|
|
XM_005259896.3:c.*6G=
|
XP_005259953.1:n.*6G=
|
|
|
NM_000215.4:c.*6G=
MANE Select
|
NP_000206.2:n.*6G=
|
|
