ENST00000398603.6:c.438dup
|
ENSP00000381604.1:p.Arg147AlafsTer16
|
|
ENST00000398606.10:c.546dup
MANE Select
|
ENSP00000381607.3:p.Arg183AlafsTer16
|
|
ENST00000646888.1:c.*262dup
|
ENSP00000494477.1:n.*262dup
|
|
ENST00000398603.5:c.438dup
|
ENSP00000381604.1:p.Arg147AlafsTer16
|
|
ENST00000398606.7:c.546dup
|
ENSP00000381607.3:p.Arg183AlafsTer16
|
|
ENST00000467591.1:n.657dup
|
|
|
ENST00000494593.1:n.1518dup
|
|
|
ENST00000498765.5:c.609dup
|
|
|
NM_000852.3:c.546dup , LRG_723t1:c.546dup
|
NP_000843.1:p.Arg183AlafsTer16
|
|
NM_000852.4:c.546dup
MANE Select
|
NP_000843.1:p.Arg183AlafsTer16
|
|