ENST00000703162.1:n.493C=
|
|
|
ENST00000281043.4:c.1144C=
MANE Select
|
ENSP00000281043.3:p.Arg382=
|
|
ENST00000638417.1:c.511C=
|
ENSP00000491476.1:p.Arg171=
|
|
ENST00000281043.3:c.1144C=
|
ENSP00000281043.3:p.Arg382=
|
|
NM_001293228.1:c.1144C=
|
NP_001280157.1:p.Arg382=
|
|
NM_001293231.1:c.511C=
|
NP_001280160.1:p.Arg171=
|
|
NM_001293233.1:c.*1079C=
|
NP_001280162.1:n.*1079C=
|
|
NM_005378.5:c.1144C=
|
NP_005369.2:p.Arg382=
|
|
NM_005378.6:c.1144C=
MANE Select
|
NP_005369.2:p.Arg382=
|
|
NM_001293228.2:c.1144C=
|
NP_001280157.1:p.Arg382=
|
|
NM_001293231.2:c.511C=
|
NP_001280160.1:p.Arg171=
|
|
NM_001293233.2:c.*1079C=
|
NP_001280162.1:n.*1079C=
|
|