ENST00000328194.8:c.3638G>A
MANE Select
|
ENSP00000328524.3:p.Gly1213Asp
|
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ENST00000525784.6:n.1500G>A
|
|
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ENST00000530780.2:c.*3464G>A
|
ENSP00000433925.1:n.*3464G>A
|
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ENST00000531747.2:n.3309G>A
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ENST00000679446.1:n.3559G>A
|
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ENST00000679458.1:n.5039G>A
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ENST00000679460.1:n.4700G>A
|
|
|
ENST00000679568.1:c.3638G>A
|
ENSP00000505860.1:p.Gly1213Asp
|
|
ENST00000679745.1:n.4143G>A
|
|
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ENST00000679773.1:n.2799G>A
|
|
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ENST00000679926.1:n.4940G>A
|
|
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ENST00000679999.1:c.*695G>A
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ENSP00000505198.1:n.*695G>A
|
|
ENST00000680252.1:c.3305G>A
|
|
|
ENST00000680294.1:c.3431G>A
|
ENSP00000506113.1:p.Gly1144Asp
|
|
ENST00000680358.1:n.2937G>A
|
|
|
ENST00000680470.1:c.*1419G>A
|
ENSP00000505975.1:n.*1419G>A
|
|
ENST00000680554.1:c.*171G>A
|
ENSP00000505621.1:n.*171G>A
|
|
ENST00000680576.1:n.5114G>A
|
|
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ENST00000680599.1:n.3679G>A
|
|
|
ENST00000680742.1:c.*171G>A
|
ENSP00000505206.1:n.*171G>A
|
|
ENST00000680791.1:n.2522G>A
|
|
|
ENST00000680885.1:n.5340G>A
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|
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ENST00000681158.1:c.3222G>A
|
|
|
ENST00000681203.1:c.3566G>A
|
ENSP00000506456.1:p.Gly1189Asp
|
|
ENST00000681371.1:n.3510G>A
|
|
|
ENST00000681425.1:n.4116G>A
|
|
|
ENST00000681639.1:n.1917G>A
|
|
|
ENST00000328194.7:c.3638G>A
|
ENSP00000328524.3:p.Gly1213Asp
|
|
ENST00000525784.5:c.574G>A
|
|
|
ENST00000527700.5:n.3200G>A
|
|
|
ENST00000528725.5:c.334G>A
|
|
|
ENST00000529977.5:n.1539G>A
|
|
|
ENST00000530044.5:c.3638G>A
|
ENSP00000435866.1:p.Gly1213Asp
|
|
ENST00000531747.1:c.874G>A
|
|
|
ENST00000533737.5:c.301G>A
|
|
|
NM_001243254.1:c.3638G>A
|
NP_001230183.1:p.Gly1213Asp
|
|
NM_015213.3:c.3638G>A
|
NP_056028.2:p.Gly1213Asp
|
|
XM_005252832.1:c.3638G>A
|
XP_005252889.1:p.Gly1213Asp
|
|
XM_011519952.1:c.3638G>A
|
XP_011518254.1:p.Gly1213Asp
|
|
XM_011519953.1:c.1736G>A
|
XP_011518255.1:p.Gly579Asp
|
|
XR_242782.2:n.3820G>A
|
|
|
XR_930851.1:n.3820G>A
|
|
|
NM_001348749.1:c.3566G>A
|
NP_001335678.1:p.Gly1189Asp
|
|
NM_001348750.1:c.3350G>A
|
NP_001335679.1:p.Gly1117Asp
|
|
NR_145966.2:n.3812G>A
|
|
|
NM_015213.4:c.3638G>A
MANE Select
|
NP_056028.2:p.Gly1213Asp
|
|
NM_001243254.2:c.3638G>A
|
NP_001230183.1:p.Gly1213Asp
|
|
NM_001348749.2:c.3566G>A
|
NP_001335678.1:p.Gly1189Asp
|
|
NM_001348750.2:c.3350G>A
|
NP_001335679.1:p.Gly1117Asp
|
|