ENST00000576204.6:n.870A>G
|
|
|
ENST00000622290.5:c.*179A>G
|
ENSP00000483331.2:n.*179A>G
|
|
ENST00000205557.12:c.4007A>G
MANE Select
|
ENSP00000205557.7:p.His1336Arg
|
|
ENST00000640696.1:c.821A>G
|
ENSP00000492197.1:p.His274Arg
|
|
ENST00000205557.11:c.4007A>G
|
ENSP00000205557.7:p.His1336Arg
|
|
ENST00000456970.6:c.3632A>G
|
ENSP00000405002.2:n.3632A>G
|
|
ENST00000576204.5:n.870A>G
|
|
|
ENST00000622290.4:c.*1216A>G
|
ENSP00000483331.1:n.*1216A>G
|
|
NM_001171.5:c.4007A>G
|
NP_001162.4:p.His1336Arg
|
|
XM_011522479.1:c.3974A>G
|
XP_011520781.1:p.His1325Arg
|
|
XM_011522480.1:c.3665A>G
|
XP_011520782.1:p.His1222Arg
|
|
XM_011522481.1:c.3665A>G
|
XP_011520783.1:p.His1222Arg
|
|
XR_933134.1:n.539-4874T>C
|
|
|
NM_001351800.1:c.3665A>G
|
NP_001338729.1:p.His1222Arg
|
|
NR_147784.1:n.3669A>G
|
|
|
XM_011522479.2:c.3974A>G
|
XP_011520781.1:p.His1325Arg
|
|
XM_011522481.3:c.3665A>G
|
XP_011520783.1:p.His1222Arg
|
|
XM_017023212.1:c.3839A>G
|
XP_016878701.1:p.His1280Arg
|
|
XM_024450261.1:c.4043A>G
|
XP_024306029.1:p.His1348Arg
|
|
NM_001171.6:c.4007A>G
MANE Select
|
NP_001162.5:p.His1336Arg
|
|