ENST00000302850.10:c.4021G>C
MANE Select
|
ENSP00000303830.4:p.Gly1341Arg
|
|
ENST00000302850.9:c.4021G>C
|
ENSP00000303830.4:p.Gly1341Arg
|
|
ENST00000341500.9:c.3985G>C
|
ENSP00000342838.4:p.Gly1329Arg
|
|
NM_000208.2:c.4021G>C
|
NP_000199.2:p.Gly1341Arg
|
|
NM_000208.3:c.4021G>C
|
NP_000199.2:p.Gly1341Arg
|
|
NM_001079817.1:c.3985G>C
|
NP_001073285.1:p.Gly1329Arg
|
|
NM_001079817.2:c.3985G>C
|
NP_001073285.1:p.Gly1329Arg
|
|
XM_011527988.1:c.4096G>C
|
XP_011526290.1:p.Gly1366Arg
|
|
XM_011527989.1:c.4060G>C
|
XP_011526291.1:p.Gly1354Arg
|
|
XM_011527988.2:c.4018G>C
|
XP_011526290.2:p.Gly1340Arg
|
|
XM_011527989.3:c.3982G>C
|
XP_011526291.2:p.Gly1328Arg
|
|
NM_000208.4:c.4021G>C
MANE Select
|
NP_000199.2:p.Gly1341Arg
|
|
NM_001079817.3:c.3985G>C
|
NP_001073285.1:p.Gly1329Arg
|
|