ENST00000302850.10:c.3253C>G
MANE Select
|
ENSP00000303830.4:p.His1085Asp
|
|
ENST00000302850.9:c.3253C>G
|
ENSP00000303830.4:p.His1085Asp
|
|
ENST00000341500.9:c.3217C>G
|
ENSP00000342838.4:p.His1073Asp
|
|
ENST00000593970.1:n.99C>G
|
|
|
NM_000208.2:c.3253C>G
|
NP_000199.2:p.His1085Asp
|
|
NM_000208.3:c.3253C>G
|
NP_000199.2:p.His1085Asp
|
|
NM_001079817.1:c.3217C>G
|
NP_001073285.1:p.His1073Asp
|
|
NM_001079817.2:c.3217C>G
|
NP_001073285.1:p.His1073Asp
|
|
XM_011527988.1:c.3328C>G
|
XP_011526290.1:p.His1110Asp
|
|
XM_011527989.1:c.3292C>G
|
XP_011526291.1:p.His1098Asp
|
|
XM_011527988.2:c.3250C>G
|
XP_011526290.2:p.His1084Asp
|
|
XM_011527989.3:c.3214C>G
|
XP_011526291.2:p.His1072Asp
|
|
NM_000208.4:c.3253C>G
MANE Select
|
NP_000199.2:p.His1085Asp
|
|
NM_001079817.3:c.3217C>G
|
NP_001073285.1:p.His1073Asp
|
|