ENST00000317961.9:c.4043A>T
MANE Select
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ENSP00000322408.4:p.Glu1348Val
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ENST00000317961.8:c.4043A>T
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ENSP00000322408.4:p.Glu1348Val
|
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ENST00000382806.6:c.3872A>T
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ENSP00000372256.2:p.Glu1291Val
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ENST00000440077.5:c.3920A>T
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ENSP00000398543.1:p.Glu1307Val
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ENST00000469599.6:n.2641A>T
|
|
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ENST00000492117.1:n.3935A>T
|
|
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ENST00000541639.5:c.4136A>T
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ENSP00000444293.1:p.Glu1379Val
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NM_001146705.1:c.4136A>T
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NP_001140177.1:p.Glu1379Val
|
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NM_001146706.1:c.3872A>T
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NP_001140178.1:p.Glu1291Val
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|
NM_004653.4:c.4043A>T
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NP_004644.2:p.Glu1348Val
|
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XM_005262560.1:c.3908A>T
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XP_005262617.1:p.Glu1303Val
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XM_005262561.1:c.3812A>T
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XP_005262618.1:p.Glu1271Val
|
|
XM_011531468.1:c.3965A>T
|
XP_011529770.1:p.Glu1322Val
|
|
XR_244571.2:n.4331A>T
|
|
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XR_430568.2:n.4665A>T
|
|
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XM_005262560.3:c.3908A>T
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XP_005262617.1:p.Glu1303Val
|
|
XM_005262561.3:c.3812A>T
|
XP_005262618.1:p.Glu1271Val
|
|
XM_011531468.3:c.3965A>T
|
XP_011529770.1:p.Glu1322Val
|
|
XM_024452495.1:c.2033A>T
|
XP_024308263.1:p.Glu678Val
|
|
XM_024452496.1:c.1799A>T
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XP_024308264.1:p.Glu600Val
|
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XR_001756009.2:n.4781A>T
|
|
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XR_001756010.2:n.4781A>T
|
|
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XR_001756011.2:n.4646A>T
|
|
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XR_001756012.2:n.4794A>T
|
|
|
XR_001756013.2:n.4112A>T
|
|
|
XR_002958832.1:n.4213A>T
|
|
|
XR_002958834.1:n.4437A>T
|
|
|
XR_002958835.1:n.4320A>T
|
|
|
XR_002958836.1:n.5003A>T
|
|
|
XR_002958837.1:n.4810A>T
|
|
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XR_244571.4:n.4330A>T
|
|
|
XR_430568.4:n.4664A>T
|
|
|
NM_001146706.2:c.3872A>T
|
NP_001140178.1:p.Glu1291Val
|
|
NM_004653.5:c.4043A>T
MANE Select
|
NP_004644.2:p.Glu1348Val
|
|
NM_001146705.2:c.4136A>T
|
NP_001140177.1:p.Glu1379Val
|
|