ENST00000302850.10:c.3222G>C
MANE Select
|
ENSP00000303830.4:p.Glu1074Asp
|
|
ENST00000302850.9:c.3222G>C
|
ENSP00000303830.4:p.Glu1074Asp
|
|
ENST00000341500.9:c.3186G>C
|
ENSP00000342838.4:p.Glu1062Asp
|
|
ENST00000593970.1:n.68G>C
|
|
|
NM_000208.2:c.3222G>C
|
NP_000199.2:p.Glu1074Asp
|
|
NM_000208.3:c.3222G>C
|
NP_000199.2:p.Glu1074Asp
|
|
NM_001079817.1:c.3186G>C
|
NP_001073285.1:p.Glu1062Asp
|
|
NM_001079817.2:c.3186G>C
|
NP_001073285.1:p.Glu1062Asp
|
|
XM_011527988.1:c.3297G>C
|
XP_011526290.1:p.Glu1099Asp
|
|
XM_011527989.1:c.3261G>C
|
XP_011526291.1:p.Glu1087Asp
|
|
XM_011527988.2:c.3219G>C
|
XP_011526290.2:p.Glu1073Asp
|
|
XM_011527989.3:c.3183G>C
|
XP_011526291.2:p.Glu1061Asp
|
|
NM_000208.4:c.3222G>C
MANE Select
|
NP_000199.2:p.Glu1074Asp
|
|
NM_001079817.3:c.3186G>C
|
NP_001073285.1:p.Glu1062Asp
|
|