ENST00000576204.6:n.879G=
|
|
|
ENST00000622290.5:c.*188G=
|
ENSP00000483331.2:n.*188G=
|
|
ENST00000205557.12:c.4016G=
MANE Select
|
ENSP00000205557.7:p.Arg1339=
|
|
ENST00000640696.1:c.830G=
|
ENSP00000492197.1:p.Arg277=
|
|
ENST00000205557.11:c.4016G=
|
ENSP00000205557.7:p.Arg1339=
|
|
ENST00000456970.6:c.3641G=
|
ENSP00000405002.2:n.3641G=
|
|
ENST00000576204.5:n.879G=
|
|
|
ENST00000622290.4:c.*1225G=
|
ENSP00000483331.1:n.*1225G=
|
|
NM_001171.5:c.4016G=
|
NP_001162.4:p.Arg1339=
|
|
XM_011522479.1:c.3983G=
|
XP_011520781.1:p.Arg1328=
|
|
XM_011522480.1:c.3674G=
|
XP_011520782.1:p.Arg1225=
|
|
XM_011522481.1:c.3674G=
|
XP_011520783.1:p.Arg1225=
|
|
XR_933134.1:n.539-4883C=
|
|
|
NM_001351800.1:c.3674G=
|
NP_001338729.1:p.Arg1225=
|
|
NR_147784.1:n.3678G=
|
|
|
XM_011522479.2:c.3983G=
|
XP_011520781.1:p.Arg1328=
|
|
XM_011522481.3:c.3674G=
|
XP_011520783.1:p.Arg1225=
|
|
XM_017023212.1:c.3848G=
|
XP_016878701.1:p.Arg1283=
|
|
XM_024450261.1:c.4052G=
|
XP_024306029.1:p.Arg1351=
|
|
NM_001171.6:c.4016G=
MANE Select
|
NP_001162.5:p.Arg1339=
|
|