ENST00000368407.8:c.500C>T
MANE Select
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ENSP00000357392.3:p.Ala167Val
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ENST00000368406.2:c.434C>T
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ENSP00000357391.2:p.Ala145Val
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ENST00000368407.7:c.500C>T
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ENSP00000357392.3:p.Ala167Val
|
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ENST00000469878.5:n.751C>T
|
|
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ENST00000474413.5:n.725C>T
|
|
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ENST00000497282.1:n.543C>T
|
|
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NM_004428.2:c.500C>T
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NP_004419.2:p.Ala167Val
|
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NM_182685.1:c.434C>T
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NP_872626.1:p.Ala145Val
|
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XM_005244940.3:c.311C>T
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XP_005244997.1:p.Ala104Val
|
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NM_004428.3:c.500C>T
MANE Select
|
NP_004419.2:p.Ala167Val
|
|
NM_182685.2:c.434C>T
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NP_872626.1:p.Ala145Val
|
|