ENST00000396705.10:c.638T>C
MANE Select
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ENSP00000379933.4:p.Val213Ala
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ENST00000229270.8:c.749T>C
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ENSP00000229270.4:p.Val250Ala
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ENST00000396705.9:c.638T>C
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ENSP00000379933.4:p.Val213Ala
|
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ENST00000474253.1:n.127T>C
|
|
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ENST00000488464.6:c.392T>C
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ENSP00000475620.1:p.Val131Ala
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ENST00000535434.5:c.392T>C
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ENSP00000443599.1:p.Val131Ala
|
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ENST00000613953.4:c.749T>C
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ENSP00000484435.1:p.Val250Ala
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NM_000365.5:c.638T>C
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NP_000356.1:p.Val213Ala
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NM_001159287.1:c.749T>C
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NP_001152759.1:p.Val250Ala
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NM_001258026.1:c.392T>C
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NP_001244955.1:p.Val131Ala
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XR_002957378.1:n.1646T>C
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|
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NM_000365.6:c.638T>C
MANE Select
|
NP_000356.1:p.Val213Ala
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NM_001258026.2:c.392T>C
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NP_001244955.1:p.Val131Ala
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