ENST00000703162.1:n.227C>T
|
|
|
ENST00000281043.4:c.878C>T
MANE Select
|
ENSP00000281043.3:p.Ala293Val
|
|
ENST00000638417.1:c.245C>T
|
ENSP00000491476.1:p.Ala82Val
|
|
ENST00000281043.3:c.878C>T
|
ENSP00000281043.3:p.Ala293Val
|
|
NM_001293228.1:c.878C>T
|
NP_001280157.1:p.Ala293Val
|
|
NM_001293231.1:c.245C>T
|
NP_001280160.1:p.Ala82Val
|
|
NM_001293233.1:c.*813C>T
|
NP_001280162.1:n.*813C>T
|
|
NM_005378.5:c.878C>T
|
NP_005369.2:p.Ala293Val
|
|
NM_005378.6:c.878C>T
MANE Select
|
NP_005369.2:p.Ala293Val
|
|
NM_001293228.2:c.878C>T
|
NP_001280157.1:p.Ala293Val
|
|
NM_001293231.2:c.245C>T
|
NP_001280160.1:p.Ala82Val
|
|
NM_001293233.2:c.*813C>T
|
NP_001280162.1:n.*813C>T
|
|