ENST00000302850.10:c.3239G=
MANE Select
|
ENSP00000303830.4:p.Gly1080=
|
|
ENST00000302850.9:c.3239G=
|
ENSP00000303830.4:p.Gly1080=
|
|
ENST00000341500.9:c.3203G=
|
ENSP00000342838.4:p.Gly1068=
|
|
ENST00000593970.1:n.85G=
|
|
|
NM_000208.2:c.3239G=
|
NP_000199.2:p.Gly1080=
|
|
NM_000208.3:c.3239G=
|
NP_000199.2:p.Gly1080=
|
|
NM_001079817.1:c.3203G=
|
NP_001073285.1:p.Gly1068=
|
|
NM_001079817.2:c.3203G=
|
NP_001073285.1:p.Gly1068=
|
|
XM_011527988.1:c.3314G=
|
XP_011526290.1:p.Gly1105=
|
|
XM_011527989.1:c.3278G=
|
XP_011526291.1:p.Gly1093=
|
|
XM_011527988.2:c.3236G=
|
XP_011526290.2:p.Gly1079=
|
|
XM_011527989.3:c.3200G=
|
XP_011526291.2:p.Gly1067=
|
|
NM_000208.4:c.3239G=
MANE Select
|
NP_000199.2:p.Gly1080=
|
|
NM_001079817.3:c.3203G=
|
NP_001073285.1:p.Gly1068=
|
|