ENST00000302850.10:c.3874G>C
MANE Select
|
ENSP00000303830.4:p.Asp1292His
|
|
ENST00000302850.9:c.3874G>C
|
ENSP00000303830.4:p.Asp1292His
|
|
ENST00000341500.9:c.3838G>C
|
ENSP00000342838.4:p.Asp1280His
|
|
NM_000208.2:c.3874G>C
|
NP_000199.2:p.Asp1292His
|
|
NM_000208.3:c.3874G>C
|
NP_000199.2:p.Asp1292His
|
|
NM_001079817.1:c.3838G>C
|
NP_001073285.1:p.Asp1280His
|
|
NM_001079817.2:c.3838G>C
|
NP_001073285.1:p.Asp1280His
|
|
XM_011527988.1:c.3949G>C
|
XP_011526290.1:p.Asp1317His
|
|
XM_011527989.1:c.3913G>C
|
XP_011526291.1:p.Asp1305His
|
|
XM_011527988.2:c.3871G>C
|
XP_011526290.2:p.Asp1291His
|
|
XM_011527989.3:c.3835G>C
|
XP_011526291.2:p.Asp1279His
|
|
NM_000208.4:c.3874G>C
MANE Select
|
NP_000199.2:p.Asp1292His
|
|
NM_001079817.3:c.3838G>C
|
NP_001073285.1:p.Asp1280His
|
|