ENST00000302850.10:c.3302T>G
MANE Select
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ENSP00000303830.4:p.Val1101Gly
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ENST00000302850.9:c.3302T>G
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ENSP00000303830.4:p.Val1101Gly
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ENST00000341500.9:c.3266T>G
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ENSP00000342838.4:p.Val1089Gly
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ENST00000593970.1:n.148T>G
|
|
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ENST00000601099.1:n.213T>G
|
|
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NM_000208.2:c.3302T>G
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NP_000199.2:p.Val1101Gly
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NM_000208.3:c.3302T>G
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NP_000199.2:p.Val1101Gly
|
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NM_001079817.1:c.3266T>G
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NP_001073285.1:p.Val1089Gly
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NM_001079817.2:c.3266T>G
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NP_001073285.1:p.Val1089Gly
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XM_011527988.1:c.3377T>G
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XP_011526290.1:p.Val1126Gly
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XM_011527989.1:c.3341T>G
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XP_011526291.1:p.Val1114Gly
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XM_011527988.2:c.3299T>G
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XP_011526290.2:p.Val1100Gly
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XM_011527989.3:c.3263T>G
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XP_011526291.2:p.Val1088Gly
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NM_000208.4:c.3302T>G
MANE Select
|
NP_000199.2:p.Val1101Gly
|
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NM_001079817.3:c.3266T>G
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NP_001073285.1:p.Val1089Gly
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