ENST00000526008.6:c.*1900G>T
|
ENSP00000513006.1:n.*1900G>T
|
|
ENST00000696967.1:n.2520G>T
|
|
|
ENST00000696968.1:n.576G>T
|
|
|
ENST00000696969.1:n.2300G>T
|
|
|
ENST00000458235.7:c.3343G>T
MANE Select
|
ENSP00000391676.1:p.Glu1115Ter
|
|
ENST00000458235.5:c.3343G>T
|
ENSP00000391676.1:p.Glu1115Ter
|
|
ENST00000527031.5:n.2279-1465G>T
|
|
|
ENST00000527670.5:c.3343G>T
|
ENSP00000432511.1:p.Glu1115Ter
|
|
NM_000215.3:c.3343G>T , LRG_77t1:c.3343G>T
|
NP_000206.2:p.Glu1115Ter
|
|
XM_005259896.2:c.3472G>T
|
XP_005259953.1:p.Glu1158Ter
|
|
XM_006722745.2:c.3343G>T
|
XP_006722808.1:p.Glu1115Ter
|
|
XM_005259896.3:c.3472G>T
|
XP_005259953.1:p.Glu1158Ter
|
|
NM_000215.4:c.3343G>T
MANE Select
|
NP_000206.2:p.Glu1115Ter
|
|