ENST00000398603.6:c.402C>A
|
ENSP00000381604.1:p.Cys134Ter
|
|
ENST00000398606.10:c.510C>A
MANE Select
|
ENSP00000381607.3:p.Cys170Ter
|
|
ENST00000646888.1:c.*226C>A
|
ENSP00000494477.1:n.*226C>A
|
|
ENST00000398603.5:c.402C>A
|
ENSP00000381604.1:p.Cys134Ter
|
|
ENST00000398606.7:c.510C>A
|
ENSP00000381607.3:p.Cys170Ter
|
|
ENST00000467591.1:n.621C>A
|
|
|
ENST00000494593.1:n.1482C>A
|
|
|
ENST00000498765.5:c.573C>A
|
|
|
NM_000852.3:c.510C>A , LRG_723t1:c.510C>A
|
NP_000843.1:p.Cys170Ter
|
|
NM_000852.4:c.510C>A
MANE Select
|
NP_000843.1:p.Cys170Ter
|
|