ENST00000302850.10:c.4025G>C
MANE Select
|
ENSP00000303830.4:p.Gly1342Ala
|
|
ENST00000302850.9:c.4025G>C
|
ENSP00000303830.4:p.Gly1342Ala
|
|
ENST00000341500.9:c.3989G>C
|
ENSP00000342838.4:p.Gly1330Ala
|
|
NM_000208.2:c.4025G>C
|
NP_000199.2:p.Gly1342Ala
|
|
NM_000208.3:c.4025G>C
|
NP_000199.2:p.Gly1342Ala
|
|
NM_001079817.1:c.3989G>C
|
NP_001073285.1:p.Gly1330Ala
|
|
NM_001079817.2:c.3989G>C
|
NP_001073285.1:p.Gly1330Ala
|
|
XM_011527988.1:c.4100G>C
|
XP_011526290.1:p.Gly1367Ala
|
|
XM_011527989.1:c.4064G>C
|
XP_011526291.1:p.Gly1355Ala
|
|
XM_011527988.2:c.4022G>C
|
XP_011526290.2:p.Gly1341Ala
|
|
XM_011527989.3:c.3986G>C
|
XP_011526291.2:p.Gly1329Ala
|
|
NM_000208.4:c.4025G>C
MANE Select
|
NP_000199.2:p.Gly1342Ala
|
|
NM_001079817.3:c.3989G>C
|
NP_001073285.1:p.Gly1330Ala
|
|