ENST00000302850.10:c.4129C=
MANE Select
|
ENSP00000303830.4:p.Pro1377=
|
|
ENST00000302850.9:c.4129C=
|
ENSP00000303830.4:p.Pro1377=
|
|
ENST00000341500.9:c.4093C=
|
ENSP00000342838.4:p.Pro1365=
|
|
NM_000208.2:c.4129C=
|
NP_000199.2:p.Pro1377=
|
|
NM_000208.3:c.4129C=
|
NP_000199.2:p.Pro1377=
|
|
NM_001079817.1:c.4093C=
|
NP_001073285.1:p.Pro1365=
|
|
NM_001079817.2:c.4093C=
|
NP_001073285.1:p.Pro1365=
|
|
XM_011527988.1:c.4204C=
|
XP_011526290.1:p.Pro1402=
|
|
XM_011527989.1:c.4168C=
|
XP_011526291.1:p.Pro1390=
|
|
XM_011527988.2:c.4126C=
|
XP_011526290.2:p.Pro1376=
|
|
XM_011527989.3:c.4090C=
|
XP_011526291.2:p.Pro1364=
|
|
NM_000208.4:c.4129C=
MANE Select
|
NP_000199.2:p.Pro1377=
|
|
NM_001079817.3:c.4093C=
|
NP_001073285.1:p.Pro1365=
|
|