ENST00000215882.10:c.704T>C
MANE Select
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ENSP00000215882.5:p.Val235Ala
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ENST00000215882.9:c.704T>C
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ENSP00000215882.5:p.Val235Ala
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ENST00000451283.5:c.395T>C
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ENSP00000401480.1:p.Val132Ala
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ENST00000470922.5:n.846T>C
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|
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NM_001256534.1:c.725T>C
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NP_001243463.1:p.Val242Ala
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NM_001287387.1:c.395T>C
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NP_001274316.1:p.Val132Ala
|
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NM_005984.4:c.704T>C
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NP_005975.1:p.Val235Ala
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NR_046298.2:n.755T>C
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|
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NM_005984.5:c.704T>C
MANE Select
|
NP_005975.1:p.Val235Ala
|
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NM_001256534.2:c.725T>C
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NP_001243463.1:p.Val242Ala
|
|
NM_001287387.2:c.395T>C
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NP_001274316.1:p.Val132Ala
|
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NR_046298.3:n.628T>C
|
|
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