ENST00000263967.4:c.3139_3140delinsCA
MANE Select
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ENSP00000263967.3:p.His1047=
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ENST00000462255.2:n.2162_2163delinsCA
|
|
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ENST00000643187.1:c.*219_*220delinsCA
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ENSP00000493507.1:n.*219_*220delinsCA
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ENST00000674534.1:n.4047_4048delinsCA
|
|
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ENST00000674622.1:c.1560_1561delinsCA
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ENSP00000502417.1:n.1560_1561delinsCA
|
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ENST00000675467.1:n.5946_5947delinsCA
|
|
|
ENST00000675786.1:c.*1706_*1707delinsCA
|
ENSP00000502323.1:n.*1706_*1707delinsCA
|
|
ENST00000675796.1:n.3034_3035delinsCA
|
|
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ENST00000263967.3:c.3139_3140delinsCA
|
ENSP00000263967.3:p.His1047=
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|
NM_006218.2:c.3139_3140delinsCA , LRG_310t1:c.3139_3140delinsCA
|
NP_006209.2:p.His1047=
|
|
XM_006713658.2:c.3139_3140delinsCA
|
XP_006713721.1:p.His1047=
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|
XM_011512894.1:c.3139_3140delinsCA
|
XP_011511196.1:p.His1047=
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|
NM_006218.3:c.3139_3140delinsCA
|
NP_006209.2:p.His1047=
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|
XM_006713658.4:c.3139_3140delinsCA
|
XP_006713721.1:p.His1047=
|
|
XM_011512894.2:c.3139_3140delinsCA
|
XP_011511196.1:p.His1047=
|
|
NM_006218.4:c.3139_3140delinsCA
MANE Select
|
NP_006209.2:p.His1047=
|
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