ENST00000684241.1:n.4167T>G
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|
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ENST00000262186.10:c.3334T>G
MANE Select
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ENSP00000262186.5:p.Ser1112Ala
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ENST00000330883.9:c.2314T>G
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ENSP00000328531.4:p.Ser772Ala
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ENST00000262186.9:c.3334T>G
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ENSP00000262186.5:p.Ser1112Ala
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ENST00000330883.8:c.2314T>G
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ENSP00000328531.4:p.Ser772Ala
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NM_000238.3:c.3334T>G , LRG_288t1:c.3334T>G
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NP_000229.1:p.Ser1112Ala
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NM_172057.2:c.2314T>G , LRG_288t3:c.2314T>G
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NP_742054.1:p.Ser772Ala
|
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XM_011516185.1:c.3034T>G
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XP_011514487.1:p.Ser1012Ala
|
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XM_011516185.2:c.3034T>G
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XP_011514487.1:p.Ser1012Ala
|
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XM_017012195.1:c.3184T>G
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XP_016867684.1:p.Ser1062Ala
|
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XM_017012196.1:c.3157T>G
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XP_016867685.1:p.Ser1053Ala
|
|
NM_000238.4:c.3334T>G
MANE Select
|
NP_000229.1:p.Ser1112Ala
|
|
NM_172057.3:c.2314T>G
|
NP_742054.1:p.Ser772Ala
|
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