ENST00000398603.6:c.366C>T
|
ENSP00000381604.1:p.Asp122=
|
|
ENST00000398606.10:c.474C>T
MANE Select
|
ENSP00000381607.3:p.Asp158=
|
|
ENST00000646888.1:c.*190C>T
|
ENSP00000494477.1:n.*190C>T
|
|
ENST00000398603.5:c.366C>T
|
ENSP00000381604.1:p.Asp122=
|
|
ENST00000398606.7:c.474C>T
|
ENSP00000381607.3:p.Asp158=
|
|
ENST00000467591.1:n.585C>T
|
|
|
ENST00000494593.1:n.1446C>T
|
|
|
ENST00000495996.1:c.200C>T
|
ENSP00000484686.1:p.Thr67Ile
|
|
ENST00000498765.5:c.537C>T
|
|
|
NM_000852.3:c.474C>T , LRG_723t1:c.474C>T
|
NP_000843.1:p.Asp158=
|
|
NM_000852.4:c.474C>T
MANE Select
|
NP_000843.1:p.Asp158=
|
|