ENST00000526008.6:c.*2029G>C
|
ENSP00000513006.1:n.*2029G>C
|
|
ENST00000696967.1:n.2649G>C
|
|
|
ENST00000696968.1:n.705G>C
|
|
|
ENST00000696969.1:n.2429G>C
|
|
|
ENST00000458235.7:c.*97G>C
MANE Select
|
ENSP00000391676.1:n.*97G>C
|
|
ENST00000458235.5:c.*97G>C
|
ENSP00000391676.1:n.*97G>C
|
|
ENST00000527031.5:n.2279-1336G>C
|
|
|
ENST00000527670.5:c.*97G>C
|
ENSP00000432511.1:n.*97G>C
|
|
NM_000215.3:c.*97G>C , LRG_77t1:c.*97G>C
|
NP_000206.2:n.*97G>C
|
|
XM_005259896.2:c.*97G>C
|
XP_005259953.1:n.*97G>C
|
|
XM_006722745.2:c.*97G>C
|
XP_006722808.1:n.*97G>C
|
|
XM_005259896.3:c.*97G>C
|
XP_005259953.1:n.*97G>C
|
|
NM_000215.4:c.*97G>C
MANE Select
|
NP_000206.2:n.*97G>C
|
|