ENST00000302850.10:c.3047G>C
MANE Select
|
ENSP00000303830.4:p.Trp1016Ser
|
|
ENST00000302850.9:c.3047G>C
|
ENSP00000303830.4:p.Trp1016Ser
|
|
ENST00000341500.9:c.3011G>C
|
ENSP00000342838.4:p.Trp1004Ser
|
|
NM_000208.2:c.3047G>C
|
NP_000199.2:p.Trp1016Ser
|
|
NM_000208.3:c.3047G>C
|
NP_000199.2:p.Trp1016Ser
|
|
NM_001079817.1:c.3011G>C
|
NP_001073285.1:p.Trp1004Ser
|
|
NM_001079817.2:c.3011G>C
|
NP_001073285.1:p.Trp1004Ser
|
|
XM_011527988.1:c.3122G>C
|
XP_011526290.1:p.Trp1041Ser
|
|
XM_011527989.1:c.3086G>C
|
XP_011526291.1:p.Trp1029Ser
|
|
XM_011527988.2:c.3044G>C
|
XP_011526290.2:p.Trp1015Ser
|
|
XM_011527989.3:c.3008G>C
|
XP_011526291.2:p.Trp1003Ser
|
|
NM_000208.4:c.3047G>C
MANE Select
|
NP_000199.2:p.Trp1016Ser
|
|
NM_001079817.3:c.3011G>C
|
NP_001073285.1:p.Trp1004Ser
|
|