ENST00000302850.10:c.3163G>T
MANE Select
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ENSP00000303830.4:p.Ala1055Ser
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ENST00000302850.9:c.3163G>T
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ENSP00000303830.4:p.Ala1055Ser
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ENST00000341500.9:c.3127G>T
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ENSP00000342838.4:p.Ala1043Ser
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ENST00000593970.1:n.9G>T
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NM_000208.2:c.3163G>T
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NP_000199.2:p.Ala1055Ser
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NM_000208.3:c.3163G>T
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NP_000199.2:p.Ala1055Ser
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NM_001079817.1:c.3127G>T
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NP_001073285.1:p.Ala1043Ser
|
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NM_001079817.2:c.3127G>T
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NP_001073285.1:p.Ala1043Ser
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XM_011527988.1:c.3238G>T
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XP_011526290.1:p.Ala1080Ser
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XM_011527989.1:c.3202G>T
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XP_011526291.1:p.Ala1068Ser
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XM_011527988.2:c.3160G>T
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XP_011526290.2:p.Ala1054Ser
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XM_011527989.3:c.3124G>T
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XP_011526291.2:p.Ala1042Ser
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NM_000208.4:c.3163G>T
MANE Select
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NP_000199.2:p.Ala1055Ser
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NM_001079817.3:c.3127G>T
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NP_001073285.1:p.Ala1043Ser
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