ENST00000302850.10:c.3237G>A
MANE Select
|
ENSP00000303830.4:p.Lys1079=
|
|
ENST00000302850.9:c.3237G>A
|
ENSP00000303830.4:p.Lys1079=
|
|
ENST00000341500.9:c.3201G>A
|
ENSP00000342838.4:p.Lys1067=
|
|
ENST00000593970.1:n.83G>A
|
|
|
NM_000208.2:c.3237G>A
|
NP_000199.2:p.Lys1079=
|
|
NM_000208.3:c.3237G>A
|
NP_000199.2:p.Lys1079=
|
|
NM_001079817.1:c.3201G>A
|
NP_001073285.1:p.Lys1067=
|
|
NM_001079817.2:c.3201G>A
|
NP_001073285.1:p.Lys1067=
|
|
XM_011527988.1:c.3312G>A
|
XP_011526290.1:p.Lys1104=
|
|
XM_011527989.1:c.3276G>A
|
XP_011526291.1:p.Lys1092=
|
|
XM_011527988.2:c.3234G>A
|
XP_011526290.2:p.Lys1078=
|
|
XM_011527989.3:c.3198G>A
|
XP_011526291.2:p.Lys1066=
|
|
NM_000208.4:c.3237G>A
MANE Select
|
NP_000199.2:p.Lys1079=
|
|
NM_001079817.3:c.3201G>A
|
NP_001073285.1:p.Lys1067=
|
|