ENST00000398603.6:c.359T>G
|
ENSP00000381604.1:p.Leu120Arg
|
|
ENST00000398606.10:c.467T>G
MANE Select
|
ENSP00000381607.3:p.Leu156Arg
|
|
ENST00000646888.1:c.*183T>G
|
ENSP00000494477.1:n.*183T>G
|
|
ENST00000398603.5:c.359T>G
|
ENSP00000381604.1:p.Leu120Arg
|
|
ENST00000398606.7:c.467T>G
|
ENSP00000381607.3:p.Leu156Arg
|
|
ENST00000467591.1:n.578T>G
|
|
|
ENST00000494593.1:n.1439T>G
|
|
|
ENST00000495996.1:c.193T>G
|
ENSP00000484686.1:p.Cys65Gly
|
|
ENST00000498765.5:c.530T>G
|
|
|
NM_000852.3:c.467T>G , LRG_723t1:c.467T>G
|
NP_000843.1:p.Leu156Arg
|
|
NM_000852.4:c.467T>G
MANE Select
|
NP_000843.1:p.Leu156Arg
|
|