ENST00000324727.9:c.367T>G
MANE Select
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ENSP00000322460.4:p.Phe123Val
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ENST00000324727.8:c.367T>G
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ENSP00000322460.4:p.Phe123Val
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ENST00000415030.6:n.510T>G
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|
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ENST00000529878.1:c.62-2593T>G
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ENSP00000436343.1:n.62-2593T>G
|
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ENST00000532138.1:n.719+58T>G
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NM_001142348.1:c.62-2593T>G
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NP_001135820.1:n.62-2593T>G
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NM_001142349.1:c.37T>G
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NP_001135821.1:p.Phe13Val
|
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NM_174934.3:c.367T>G , LRG_330t1:c.367T>G
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NP_777594.1:p.Phe123Val
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NR_024527.1:n.488+58T>G
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|
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NM_001142348.2:c.62-2593T>G
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NP_001135820.1:n.62-2593T>G
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NM_001142349.2:c.37T>G
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NP_001135821.1:p.Phe13Val
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NR_024527.2:n.452+58T>G
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|
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NM_174934.4:c.367T>G
MANE Select
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NP_777594.1:p.Phe123Val
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