ENST00000371375.2:c.4154A>C
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ENSP00000360426.1:p.Glu1385Ala
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ENST00000685253.1:c.*1621A>C
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ENSP00000509405.1:n.*1621A>C
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ENST00000685889.1:n.1813A>C
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ENST00000686807.1:n.497A>C
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ENST00000686954.1:c.*362A>C
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ENSP00000508416.1:n.*362A>C
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ENST00000688810.1:c.4106A>C
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ENSP00000509140.1:p.Glu1369Ala
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ENST00000689233.1:n.9286A>C
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ENST00000690340.1:n.2751A>C
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ENST00000692286.1:c.5036-4829A>C
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ENSP00000509490.1:n.5036-4829A>C
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ENST00000692396.1:c.5030A>C
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ENSP00000508605.1:p.Glu1677Ala
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ENST00000371380.8:c.5078A>C
MANE Select
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ENSP00000360431.2:p.Glu1693Ala
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ENST00000371385.8:c.4052A>C
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ENSP00000360438.4:p.Glu1351Ala
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ENST00000674738.1:c.3633A>C
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ENST00000674827.1:c.3194A>C
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ENSP00000502523.1:p.Glu1065Ala
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ENST00000675218.1:c.4154A>C
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ENSP00000501910.1:p.Glu1385Ala
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ENST00000675487.1:c.*1011A>C
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ENSP00000502340.1:n.*1011A>C
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ENST00000675718.1:c.4347A>C
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ENST00000676102.1:c.3923A>C
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ENSP00000502811.1:p.Glu1308Ala
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ENST00000260766.7:c.5078A>C
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ENSP00000260766.3:p.Glu1693Ala
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ENST00000371375.1:c.4154A>C
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ENSP00000360426.1:p.Glu1385Ala
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ENST00000371380.7:c.5078A>C
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ENSP00000360431.2:p.Glu1693Ala
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ENST00000371385.7:c.4154A>C
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ENSP00000360438.3:p.Glu1385Ala
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NM_001165979.2:c.4154A>C
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NP_001159451.1:p.Glu1385Ala
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NM_001288989.1:c.5030A>C
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NP_001275918.1:p.Glu1677Ala
|
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NM_016341.3:c.5078A>C
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NP_057425.3:p.Glu1693Ala
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XM_006717885.2:c.5120A>C
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XP_006717948.1:p.Glu1707Ala
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XM_006717886.2:c.5120A>C
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XP_006717949.1:p.Glu1707Ala
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XM_006717888.2:c.5117A>C
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XP_006717951.1:p.Glu1706Ala
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XM_006717889.2:c.5072A>C
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XP_006717952.1:p.Glu1691Ala
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XM_006717890.1:c.4196A>C
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XP_006717953.1:p.Glu1399Ala
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XM_011539849.1:c.5120A>C
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XP_011538151.1:p.Glu1707Ala
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XM_011539850.1:c.3965A>C
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XP_011538152.1:p.Glu1322Ala
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XM_006717885.4:c.5120A>C
|
XP_006717948.1:p.Glu1707Ala
|
|
XM_006717888.4:c.5117A>C
|
XP_006717951.1:p.Glu1706Ala
|
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XM_006717889.4:c.5072A>C
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XP_006717952.1:p.Glu1691Ala
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XM_006717890.3:c.4196A>C
|
XP_006717953.1:p.Glu1399Ala
|
|
XM_011539849.3:c.5120A>C
|
XP_011538151.1:p.Glu1707Ala
|
|
XM_011539850.3:c.3965A>C
|
XP_011538152.1:p.Glu1322Ala
|
|
XM_017016310.2:c.5120A>C
|
XP_016871799.1:p.Glu1707Ala
|
|
XM_017016311.2:c.5120A>C
|
XP_016871800.1:p.Glu1707Ala
|
|
XM_017016312.2:c.4106A>C
|
XP_016871801.1:p.Glu1369Ala
|
|
NM_001288989.2:c.5030A>C
|
NP_001275918.1:p.Glu1677Ala
|
|
NM_016341.4:c.5078A>C
MANE Select
|
NP_057425.3:p.Glu1693Ala
|
|