ENST00000302850.10:c.4020G>C
MANE Select
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ENSP00000303830.4:p.Ala1340=
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ENST00000302850.9:c.4020G>C
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ENSP00000303830.4:p.Ala1340=
|
|
ENST00000341500.9:c.3984G>C
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ENSP00000342838.4:p.Ala1328=
|
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NM_000208.2:c.4020G>C
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NP_000199.2:p.Ala1340=
|
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NM_000208.3:c.4020G>C
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NP_000199.2:p.Ala1340=
|
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NM_001079817.1:c.3984G>C
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NP_001073285.1:p.Ala1328=
|
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NM_001079817.2:c.3984G>C
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NP_001073285.1:p.Ala1328=
|
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XM_011527988.1:c.4095G>C
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XP_011526290.1:p.Ala1365=
|
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XM_011527989.1:c.4059G>C
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XP_011526291.1:p.Ala1353=
|
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XM_011527988.2:c.4017G>C
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XP_011526290.2:p.Ala1339=
|
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XM_011527989.3:c.3981G>C
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XP_011526291.2:p.Ala1327=
|
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NM_000208.4:c.4020G>C
MANE Select
|
NP_000199.2:p.Ala1340=
|
|
NM_001079817.3:c.3984G>C
|
NP_001073285.1:p.Ala1328=
|
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