ENST00000398603.6:c.372G>T
|
ENSP00000381604.1:p.Leu124=
|
|
ENST00000398606.10:c.480G>T
MANE Select
|
ENSP00000381607.3:p.Leu160=
|
|
ENST00000646888.1:c.*196G>T
|
ENSP00000494477.1:n.*196G>T
|
|
ENST00000398603.5:c.372G>T
|
ENSP00000381604.1:p.Leu124=
|
|
ENST00000398606.7:c.480G>T
|
ENSP00000381607.3:p.Leu160=
|
|
ENST00000467591.1:n.591G>T
|
|
|
ENST00000494593.1:n.1452G>T
|
|
|
ENST00000495996.1:c.206G>T
|
ENSP00000484686.1:p.Cys69Phe
|
|
ENST00000498765.5:c.543G>T
|
|
|
NM_000852.3:c.480G>T , LRG_723t1:c.480G>T
|
NP_000843.1:p.Leu160=
|
|
NM_000852.4:c.480G>T
MANE Select
|
NP_000843.1:p.Leu160=
|
|