ENST00000302850.10:c.3967G>C
MANE Select
|
ENSP00000303830.4:p.Asp1323His
|
|
ENST00000302850.9:c.3967G>C
|
ENSP00000303830.4:p.Asp1323His
|
|
ENST00000341500.9:c.3931G>C
|
ENSP00000342838.4:p.Asp1311His
|
|
NM_000208.2:c.3967G>C
|
NP_000199.2:p.Asp1323His
|
|
NM_000208.3:c.3967G>C
|
NP_000199.2:p.Asp1323His
|
|
NM_001079817.1:c.3931G>C
|
NP_001073285.1:p.Asp1311His
|
|
NM_001079817.2:c.3931G>C
|
NP_001073285.1:p.Asp1311His
|
|
XM_011527988.1:c.4042G>C
|
XP_011526290.1:p.Asp1348His
|
|
XM_011527989.1:c.4006G>C
|
XP_011526291.1:p.Asp1336His
|
|
XM_011527988.2:c.3964G>C
|
XP_011526290.2:p.Asp1322His
|
|
XM_011527989.3:c.3928G>C
|
XP_011526291.2:p.Asp1310His
|
|
NM_000208.4:c.3967G>C
MANE Select
|
NP_000199.2:p.Asp1323His
|
|
NM_001079817.3:c.3931G>C
|
NP_001073285.1:p.Asp1311His
|
|