ENST00000302850.10:c.3104G=
MANE Select
|
ENSP00000303830.4:p.Gly1035=
|
|
ENST00000302850.9:c.3104G=
|
ENSP00000303830.4:p.Gly1035=
|
|
ENST00000341500.9:c.3068G=
|
ENSP00000342838.4:p.Gly1023=
|
|
NM_000208.2:c.3104G=
|
NP_000199.2:p.Gly1035=
|
|
NM_000208.3:c.3104G=
|
NP_000199.2:p.Gly1035=
|
|
NM_001079817.1:c.3068G=
|
NP_001073285.1:p.Gly1023=
|
|
NM_001079817.2:c.3068G=
|
NP_001073285.1:p.Gly1023=
|
|
XM_011527988.1:c.3179G=
|
XP_011526290.1:p.Gly1060=
|
|
XM_011527989.1:c.3143G=
|
XP_011526291.1:p.Gly1048=
|
|
XM_011527988.2:c.3101G=
|
XP_011526290.2:p.Gly1034=
|
|
XM_011527989.3:c.3065G=
|
XP_011526291.2:p.Gly1022=
|
|
NM_000208.4:c.3104G=
MANE Select
|
NP_000199.2:p.Gly1035=
|
|
NM_001079817.3:c.3068G=
|
NP_001073285.1:p.Gly1023=
|
|