ENST00000302850.10:c.4097G>C
MANE Select
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ENSP00000303830.4:p.Gly1366Ala
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ENST00000302850.9:c.4097G>C
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ENSP00000303830.4:p.Gly1366Ala
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ENST00000341500.9:c.4061G>C
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ENSP00000342838.4:p.Gly1354Ala
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NM_000208.2:c.4097G>C
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NP_000199.2:p.Gly1366Ala
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NM_000208.3:c.4097G>C
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NP_000199.2:p.Gly1366Ala
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NM_001079817.1:c.4061G>C
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NP_001073285.1:p.Gly1354Ala
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NM_001079817.2:c.4061G>C
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NP_001073285.1:p.Gly1354Ala
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XM_011527988.1:c.4172G>C
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XP_011526290.1:p.Gly1391Ala
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XM_011527989.1:c.4136G>C
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XP_011526291.1:p.Gly1379Ala
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XM_011527988.2:c.4094G>C
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XP_011526290.2:p.Gly1365Ala
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XM_011527989.3:c.4058G>C
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XP_011526291.2:p.Gly1353Ala
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NM_000208.4:c.4097G>C
MANE Select
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NP_000199.2:p.Gly1366Ala
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NM_001079817.3:c.4061G>C
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NP_001073285.1:p.Gly1354Ala
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