ENST00000242317.9:c.1856C>T
MANE Select
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ENSP00000242317.4:p.Ala619Val
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ENST00000242317.8:c.1856C>T
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ENSP00000242317.4:p.Ala619Val
|
|
ENST00000442556.1:c.329+2583C>T
|
|
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ENST00000470169.5:c.644C>T
|
|
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ENST00000485580.1:n.432C>T
|
|
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ENST00000614641.4:c.1868C>T
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ENSP00000480538.1:p.Ala623Val
|
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NM_001281428.1:c.1868C>T
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NP_001268357.1:p.Ala623Val
|
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NM_012144.3:c.1856C>T
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NP_036276.1:p.Ala619Val
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XM_006716758.2:c.1325C>T
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XP_006716821.1:p.Ala442Val
|
|
XM_011517848.1:c.1610C>T
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XP_011516150.1:p.Ala537Val
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XM_006716758.3:c.1325C>T
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XP_006716821.1:p.Ala442Val
|
|
XM_011517848.2:c.1610C>T
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XP_011516150.1:p.Ala537Val
|
|
XM_017014625.2:c.1598C>T
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XP_016870114.1:p.Ala533Val
|
|
XR_002956774.1:n.1959C>T
|
|
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NM_012144.4:c.1856C>T
MANE Select
|
NP_036276.1:p.Ala619Val
|
|
NM_001281428.2:c.1868C>T
|
NP_001268357.1:p.Ala623Val
|
|