ENST00000302850.10:c.3201G>C
MANE Select
|
ENSP00000303830.4:p.Glu1067Asp
|
|
ENST00000302850.9:c.3201G>C
|
ENSP00000303830.4:p.Glu1067Asp
|
|
ENST00000341500.9:c.3165G>C
|
ENSP00000342838.4:p.Glu1055Asp
|
|
ENST00000593970.1:n.47G>C
|
|
|
NM_000208.2:c.3201G>C
|
NP_000199.2:p.Glu1067Asp
|
|
NM_000208.3:c.3201G>C
|
NP_000199.2:p.Glu1067Asp
|
|
NM_001079817.1:c.3165G>C
|
NP_001073285.1:p.Glu1055Asp
|
|
NM_001079817.2:c.3165G>C
|
NP_001073285.1:p.Glu1055Asp
|
|
XM_011527988.1:c.3276G>C
|
XP_011526290.1:p.Glu1092Asp
|
|
XM_011527989.1:c.3240G>C
|
XP_011526291.1:p.Glu1080Asp
|
|
XM_011527988.2:c.3198G>C
|
XP_011526290.2:p.Glu1066Asp
|
|
XM_011527989.3:c.3162G>C
|
XP_011526291.2:p.Glu1054Asp
|
|
NM_000208.4:c.3201G>C
MANE Select
|
NP_000199.2:p.Glu1067Asp
|
|
NM_001079817.3:c.3165G>C
|
NP_001073285.1:p.Glu1055Asp
|
|