ENST00000302850.10:c.3047G>A
MANE Select
|
ENSP00000303830.4:p.Trp1016Ter
|
|
ENST00000302850.9:c.3047G>A
|
ENSP00000303830.4:p.Trp1016Ter
|
|
ENST00000341500.9:c.3011G>A
|
ENSP00000342838.4:p.Trp1004Ter
|
|
NM_000208.2:c.3047G>A
|
NP_000199.2:p.Trp1016Ter
|
|
NM_000208.3:c.3047G>A
|
NP_000199.2:p.Trp1016Ter
|
|
NM_001079817.1:c.3011G>A
|
NP_001073285.1:p.Trp1004Ter
|
|
NM_001079817.2:c.3011G>A
|
NP_001073285.1:p.Trp1004Ter
|
|
XM_011527988.1:c.3122G>A
|
XP_011526290.1:p.Trp1041Ter
|
|
XM_011527989.1:c.3086G>A
|
XP_011526291.1:p.Trp1029Ter
|
|
XM_011527988.2:c.3044G>A
|
XP_011526290.2:p.Trp1015Ter
|
|
XM_011527989.3:c.3008G>A
|
XP_011526291.2:p.Trp1003Ter
|
|
NM_000208.4:c.3047G>A
MANE Select
|
NP_000199.2:p.Trp1016Ter
|
|
NM_001079817.3:c.3011G>A
|
NP_001073285.1:p.Trp1004Ter
|
|