ENST00000302850.10:c.4019C>G
MANE Select
|
ENSP00000303830.4:p.Ala1340Gly
|
|
ENST00000302850.9:c.4019C>G
|
ENSP00000303830.4:p.Ala1340Gly
|
|
ENST00000341500.9:c.3983C>G
|
ENSP00000342838.4:p.Ala1328Gly
|
|
NM_000208.2:c.4019C>G
|
NP_000199.2:p.Ala1340Gly
|
|
NM_000208.3:c.4019C>G
|
NP_000199.2:p.Ala1340Gly
|
|
NM_001079817.1:c.3983C>G
|
NP_001073285.1:p.Ala1328Gly
|
|
NM_001079817.2:c.3983C>G
|
NP_001073285.1:p.Ala1328Gly
|
|
XM_011527988.1:c.4094C>G
|
XP_011526290.1:p.Ala1365Gly
|
|
XM_011527989.1:c.4058C>G
|
XP_011526291.1:p.Ala1353Gly
|
|
XM_011527988.2:c.4016C>G
|
XP_011526290.2:p.Ala1339Gly
|
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XM_011527989.3:c.3980C>G
|
XP_011526291.2:p.Ala1327Gly
|
|
NM_000208.4:c.4019C>G
MANE Select
|
NP_000199.2:p.Ala1340Gly
|
|
NM_001079817.3:c.3983C>G
|
NP_001073285.1:p.Ala1328Gly
|
|