ENST00000703162.1:n.306C>G
|
|
|
ENST00000281043.4:c.957C>G
MANE Select
|
ENSP00000281043.3:p.Ile319Met
|
|
ENST00000638417.1:c.324C>G
|
ENSP00000491476.1:p.Ile108Met
|
|
ENST00000281043.3:c.957C>G
|
ENSP00000281043.3:p.Ile319Met
|
|
NM_001293228.1:c.957C>G
|
NP_001280157.1:p.Ile319Met
|
|
NM_001293231.1:c.324C>G
|
NP_001280160.1:p.Ile108Met
|
|
NM_001293233.1:c.*892C>G
|
NP_001280162.1:n.*892C>G
|
|
NM_005378.5:c.957C>G
|
NP_005369.2:p.Ile319Met
|
|
NM_005378.6:c.957C>G
MANE Select
|
NP_005369.2:p.Ile319Met
|
|
NM_001293228.2:c.957C>G
|
NP_001280157.1:p.Ile319Met
|
|
NM_001293231.2:c.324C>G
|
NP_001280160.1:p.Ile108Met
|
|
NM_001293233.2:c.*892C>G
|
NP_001280162.1:n.*892C>G
|
|