ENST00000302850.10:c.3116A>G
MANE Select
|
ENSP00000303830.4:p.Glu1039Gly
|
|
ENST00000302850.9:c.3116A>G
|
ENSP00000303830.4:p.Glu1039Gly
|
|
ENST00000341500.9:c.3080A>G
|
ENSP00000342838.4:p.Glu1027Gly
|
|
NM_000208.2:c.3116A>G
|
NP_000199.2:p.Glu1039Gly
|
|
NM_000208.3:c.3116A>G
|
NP_000199.2:p.Glu1039Gly
|
|
NM_001079817.1:c.3080A>G
|
NP_001073285.1:p.Glu1027Gly
|
|
NM_001079817.2:c.3080A>G
|
NP_001073285.1:p.Glu1027Gly
|
|
XM_011527988.1:c.3191A>G
|
XP_011526290.1:p.Glu1064Gly
|
|
XM_011527989.1:c.3155A>G
|
XP_011526291.1:p.Glu1052Gly
|
|
XM_011527988.2:c.3113A>G
|
XP_011526290.2:p.Glu1038Gly
|
|
XM_011527989.3:c.3077A>G
|
XP_011526291.2:p.Glu1026Gly
|
|
NM_000208.4:c.3116A>G
MANE Select
|
NP_000199.2:p.Glu1039Gly
|
|
NM_001079817.3:c.3080A>G
|
NP_001073285.1:p.Glu1027Gly
|
|