ENST00000302850.10:c.3093G>T
MANE Select
|
ENSP00000303830.4:p.Gln1031His
|
|
ENST00000302850.9:c.3093G>T
|
ENSP00000303830.4:p.Gln1031His
|
|
ENST00000341500.9:c.3057G>T
|
ENSP00000342838.4:p.Gln1019His
|
|
NM_000208.2:c.3093G>T
|
NP_000199.2:p.Gln1031His
|
|
NM_000208.3:c.3093G>T
|
NP_000199.2:p.Gln1031His
|
|
NM_001079817.1:c.3057G>T
|
NP_001073285.1:p.Gln1019His
|
|
NM_001079817.2:c.3057G>T
|
NP_001073285.1:p.Gln1019His
|
|
XM_011527988.1:c.3168G>T
|
XP_011526290.1:p.Gln1056His
|
|
XM_011527989.1:c.3132G>T
|
XP_011526291.1:p.Gln1044His
|
|
XM_011527988.2:c.3090G>T
|
XP_011526290.2:p.Gln1030His
|
|
XM_011527989.3:c.3054G>T
|
XP_011526291.2:p.Gln1018His
|
|
NM_000208.4:c.3093G>T
MANE Select
|
NP_000199.2:p.Gln1031His
|
|
NM_001079817.3:c.3057G>T
|
NP_001073285.1:p.Gln1019His
|
|