ENST00000703162.1:n.531C>T
|
|
|
ENST00000281043.4:c.1182C>T
MANE Select
|
ENSP00000281043.3:p.Arg394=
|
|
ENST00000638417.1:c.549C>T
|
ENSP00000491476.1:p.Arg183=
|
|
ENST00000281043.3:c.1182C>T
|
ENSP00000281043.3:p.Arg394=
|
|
NM_001293228.1:c.1182C>T
|
NP_001280157.1:p.Arg394=
|
|
NM_001293231.1:c.549C>T
|
NP_001280160.1:p.Arg183=
|
|
NM_001293233.1:c.*1117C>T
|
NP_001280162.1:n.*1117C>T
|
|
NM_005378.5:c.1182C>T
|
NP_005369.2:p.Arg394=
|
|
NM_005378.6:c.1182C>T
MANE Select
|
NP_005369.2:p.Arg394=
|
|
NM_001293228.2:c.1182C>T
|
NP_001280157.1:p.Arg394=
|
|
NM_001293231.2:c.549C>T
|
NP_001280160.1:p.Arg183=
|
|
NM_001293233.2:c.*1117C>T
|
NP_001280162.1:n.*1117C>T
|
|