ENST00000398603.6:c.375G>T
|
ENSP00000381604.1:p.Leu125=
|
|
ENST00000398606.10:c.483G>T
MANE Select
|
ENSP00000381607.3:p.Leu161=
|
|
ENST00000646888.1:c.*199G>T
|
ENSP00000494477.1:n.*199G>T
|
|
ENST00000398603.5:c.375G>T
|
ENSP00000381604.1:p.Leu125=
|
|
ENST00000398606.7:c.483G>T
|
ENSP00000381607.3:p.Leu161=
|
|
ENST00000467591.1:n.594G>T
|
|
|
ENST00000494593.1:n.1455G>T
|
|
|
ENST00000495996.1:c.209G>T
|
ENSP00000484686.1:p.Ter70Leu
|
|
ENST00000498765.5:c.546G>T
|
|
|
NM_000852.3:c.483G>T , LRG_723t1:c.483G>T
|
NP_000843.1:p.Leu161=
|
|
NM_000852.4:c.483G>T
MANE Select
|
NP_000843.1:p.Leu161=
|
|