ENST00000398603.6:c.449C>G
|
ENSP00000381604.1:p.Ala150Gly
|
|
ENST00000398606.10:c.557C>G
MANE Select
|
ENSP00000381607.3:p.Ala186Gly
|
|
ENST00000646888.1:c.*273C>G
|
ENSP00000494477.1:n.*273C>G
|
|
ENST00000398603.5:c.449C>G
|
ENSP00000381604.1:p.Ala150Gly
|
|
ENST00000398606.7:c.557C>G
|
ENSP00000381607.3:p.Ala186Gly
|
|
ENST00000467591.1:n.668C>G
|
|
|
ENST00000494593.1:n.1529C>G
|
|
|
ENST00000498765.5:c.620C>G
|
|
|
NM_000852.3:c.557C>G , LRG_723t1:c.557C>G
|
NP_000843.1:p.Ala186Gly
|
|
NM_000852.4:c.557C>G
MANE Select
|
NP_000843.1:p.Ala186Gly
|
|