ENST00000302850.10:c.3971T>G
MANE Select
|
ENSP00000303830.4:p.Met1324Arg
|
|
ENST00000302850.9:c.3971T>G
|
ENSP00000303830.4:p.Met1324Arg
|
|
ENST00000341500.9:c.3935T>G
|
ENSP00000342838.4:p.Met1312Arg
|
|
NM_000208.2:c.3971T>G
|
NP_000199.2:p.Met1324Arg
|
|
NM_000208.3:c.3971T>G
|
NP_000199.2:p.Met1324Arg
|
|
NM_001079817.1:c.3935T>G
|
NP_001073285.1:p.Met1312Arg
|
|
NM_001079817.2:c.3935T>G
|
NP_001073285.1:p.Met1312Arg
|
|
XM_011527988.1:c.4046T>G
|
XP_011526290.1:p.Met1349Arg
|
|
XM_011527989.1:c.4010T>G
|
XP_011526291.1:p.Met1337Arg
|
|
XM_011527988.2:c.3968T>G
|
XP_011526290.2:p.Met1323Arg
|
|
XM_011527989.3:c.3932T>G
|
XP_011526291.2:p.Met1311Arg
|
|
NM_000208.4:c.3971T>G
MANE Select
|
NP_000199.2:p.Met1324Arg
|
|
NM_001079817.3:c.3935T>G
|
NP_001073285.1:p.Met1312Arg
|
|