ENST00000398603.6:c.415C>G
|
ENSP00000381604.1:p.Pro139Ala
|
|
ENST00000398606.10:c.523C>G
MANE Select
|
ENSP00000381607.3:p.Pro175Ala
|
|
ENST00000646888.1:c.*239C>G
|
ENSP00000494477.1:n.*239C>G
|
|
ENST00000398603.5:c.415C>G
|
ENSP00000381604.1:p.Pro139Ala
|
|
ENST00000398606.7:c.523C>G
|
ENSP00000381607.3:p.Pro175Ala
|
|
ENST00000467591.1:n.634C>G
|
|
|
ENST00000494593.1:n.1495C>G
|
|
|
ENST00000498765.5:c.586C>G
|
|
|
NM_000852.3:c.523C>G , LRG_723t1:c.523C>G
|
NP_000843.1:p.Pro175Ala
|
|
NM_000852.4:c.523C>G
MANE Select
|
NP_000843.1:p.Pro175Ala
|
|