ENST00000302850.10:c.3256G=
MANE Select
|
ENSP00000303830.4:p.Val1086=
|
|
ENST00000302850.9:c.3256G=
|
ENSP00000303830.4:p.Val1086=
|
|
ENST00000341500.9:c.3220G=
|
ENSP00000342838.4:p.Val1074=
|
|
ENST00000593970.1:n.102G=
|
|
|
NM_000208.2:c.3256G=
|
NP_000199.2:p.Val1086=
|
|
NM_000208.3:c.3256G=
|
NP_000199.2:p.Val1086=
|
|
NM_001079817.1:c.3220G=
|
NP_001073285.1:p.Val1074=
|
|
NM_001079817.2:c.3220G=
|
NP_001073285.1:p.Val1074=
|
|
XM_011527988.1:c.3331G=
|
XP_011526290.1:p.Val1111=
|
|
XM_011527989.1:c.3295G=
|
XP_011526291.1:p.Val1099=
|
|
XM_011527988.2:c.3253G=
|
XP_011526290.2:p.Val1085=
|
|
XM_011527989.3:c.3217G=
|
XP_011526291.2:p.Val1073=
|
|
NM_000208.4:c.3256G=
MANE Select
|
NP_000199.2:p.Val1086=
|
|
NM_001079817.3:c.3220G=
|
NP_001073285.1:p.Val1074=
|
|