ENST00000398603.6:c.392C>G
|
ENSP00000381604.1:p.Ala131Gly
|
|
ENST00000398606.10:c.500C>G
MANE Select
|
ENSP00000381607.3:p.Ala167Gly
|
|
ENST00000646888.1:c.*216C>G
|
ENSP00000494477.1:n.*216C>G
|
|
ENST00000398603.5:c.392C>G
|
ENSP00000381604.1:p.Ala131Gly
|
|
ENST00000398606.7:c.500C>G
|
ENSP00000381607.3:p.Ala167Gly
|
|
ENST00000467591.1:n.611C>G
|
|
|
ENST00000494593.1:n.1472C>G
|
|
|
ENST00000498765.5:c.563C>G
|
|
|
NM_000852.3:c.500C>G , LRG_723t1:c.500C>G
|
NP_000843.1:p.Ala167Gly
|
|
NM_000852.4:c.500C>G
MANE Select
|
NP_000843.1:p.Ala167Gly
|
|