ENST00000398603.6:c.374T=
|
ENSP00000381604.1:p.Leu125=
|
|
ENST00000398606.10:c.482T=
MANE Select
|
ENSP00000381607.3:p.Leu161=
|
|
ENST00000646888.1:c.*198T=
|
ENSP00000494477.1:n.*198T=
|
|
ENST00000398603.5:c.374T=
|
ENSP00000381604.1:p.Leu125=
|
|
ENST00000398606.7:c.482T=
|
ENSP00000381607.3:p.Leu161=
|
|
ENST00000467591.1:n.593T=
|
|
|
ENST00000494593.1:n.1454T=
|
|
|
ENST00000495996.1:c.208T=
|
ENSP00000484686.1:p.Ter70=
|
|
ENST00000498765.5:c.545T=
|
|
|
NM_000852.3:c.482T= , LRG_723t1:c.482T=
|
NP_000843.1:p.Leu161=
|
|
NM_000852.4:c.482T=
MANE Select
|
NP_000843.1:p.Leu161=
|
|