ENST00000526008.6:c.*2068G>T
|
ENSP00000513006.1:n.*2068G>T
|
|
ENST00000696967.1:n.2688G>T
|
|
|
ENST00000696968.1:n.744G>T
|
|
|
ENST00000696969.1:n.2468G>T
|
|
|
ENST00000458235.7:c.*136G>T
MANE Select
|
ENSP00000391676.1:n.*136G>T
|
|
ENST00000458235.5:c.*136G>T
|
ENSP00000391676.1:n.*136G>T
|
|
ENST00000527031.5:n.2279-1297G>T
|
|
|
ENST00000527670.5:c.*136G>T
|
ENSP00000432511.1:n.*136G>T
|
|
NM_000215.3:c.*136G>T , LRG_77t1:c.*136G>T
|
NP_000206.2:n.*136G>T
|
|
XM_005259896.2:c.*136G>T
|
XP_005259953.1:n.*136G>T
|
|
XM_006722745.2:c.*136G>T
|
XP_006722808.1:n.*136G>T
|
|
XM_005259896.3:c.*136G>T
|
XP_005259953.1:n.*136G>T
|
|
NM_000215.4:c.*136G>T
MANE Select
|
NP_000206.2:n.*136G>T
|
|