ENST00000302850.10:c.4012G>C
MANE Select
|
ENSP00000303830.4:p.Glu1338Gln
|
|
ENST00000302850.9:c.4012G>C
|
ENSP00000303830.4:p.Glu1338Gln
|
|
ENST00000341500.9:c.3976G>C
|
ENSP00000342838.4:p.Glu1326Gln
|
|
NM_000208.2:c.4012G>C
|
NP_000199.2:p.Glu1338Gln
|
|
NM_000208.3:c.4012G>C
|
NP_000199.2:p.Glu1338Gln
|
|
NM_001079817.1:c.3976G>C
|
NP_001073285.1:p.Glu1326Gln
|
|
NM_001079817.2:c.3976G>C
|
NP_001073285.1:p.Glu1326Gln
|
|
XM_011527988.1:c.4087G>C
|
XP_011526290.1:p.Glu1363Gln
|
|
XM_011527989.1:c.4051G>C
|
XP_011526291.1:p.Glu1351Gln
|
|
XM_011527988.2:c.4009G>C
|
XP_011526290.2:p.Glu1337Gln
|
|
XM_011527989.3:c.3973G>C
|
XP_011526291.2:p.Glu1325Gln
|
|
NM_000208.4:c.4012G>C
MANE Select
|
NP_000199.2:p.Glu1338Gln
|
|
NM_001079817.3:c.3976G>C
|
NP_001073285.1:p.Glu1326Gln
|
|