ENST00000398603.6:c.442C>G
|
ENSP00000381604.1:p.Leu148Val
|
|
ENST00000398606.10:c.550C>G
MANE Select
|
ENSP00000381607.3:p.Leu184Val
|
|
ENST00000646888.1:c.*266C>G
|
ENSP00000494477.1:n.*266C>G
|
|
ENST00000398603.5:c.442C>G
|
ENSP00000381604.1:p.Leu148Val
|
|
ENST00000398606.7:c.550C>G
|
ENSP00000381607.3:p.Leu184Val
|
|
ENST00000467591.1:n.661C>G
|
|
|
ENST00000494593.1:n.1522C>G
|
|
|
ENST00000498765.5:c.613C>G
|
|
|
NM_000852.3:c.550C>G , LRG_723t1:c.550C>G
|
NP_000843.1:p.Leu184Val
|
|
NM_000852.4:c.550C>G
MANE Select
|
NP_000843.1:p.Leu184Val
|
|