ENST00000343139.11:c.428T>G
MANE Select
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ENSP00000339398.5:p.Val143Gly
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ENST00000343139.9:c.428T>G
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ENSP00000339398.5:p.Val143Gly
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ENST00000374949.2:c.428T>G
|
ENSP00000364087.2:p.Val143Gly
|
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ENST00000395363.5:c.428T>G
|
ENSP00000378767.1:p.Val143Gly
|
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ENST00000460633.1:n.456T>G
|
|
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ENST00000482745.5:c.*1260T>G
|
ENSP00000436546.1:n.*1260T>G
|
|
ENST00000496318.5:c.428T>G
|
ENSP00000437302.1:p.Val143Gly
|
|
NM_002122.3:c.428T>G
|
NP_002113.2:p.Val143Gly
|
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XM_006715079.2:c.428T>G
|
XP_006715142.1:p.Val143Gly
|
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XM_006715079.4:c.428T>G
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XP_006715142.1:p.Val143Gly
|
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XR_001744085.1:n.86+520A>C
|
|
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NM_002122.5:c.428T>G
MANE Select
|
NP_002113.2:p.Val143Gly
|
|