ENST00000682338.1:c.1775G>C
|
ENSP00000507062.1:p.Gly592Ala
|
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ENST00000682793.1:c.1775G>C
|
ENSP00000506910.1:p.Gly592Ala
|
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ENST00000682838.1:c.*1517G>C
|
ENSP00000507652.1:n.*1517G>C
|
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ENST00000683578.1:c.1775G>C
|
ENSP00000507430.1:p.Gly592Ala
|
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ENST00000683606.1:n.1381G>C
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|
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ENST00000683661.1:n.3310G>C
|
|
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ENST00000684324.1:c.1775G>C
|
ENSP00000507937.1:p.Gly592Ala
|
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ENST00000684545.1:c.1775G>C
|
ENSP00000506733.1:p.Gly592Ala
|
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ENST00000684624.1:n.1152G>C
|
|
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ENST00000684714.1:c.1726G>C
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ENSP00000506861.1:p.Ala576Pro
|
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ENST00000684731.1:n.1102G>C
|
|
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ENST00000375679.9:c.1775G>C
MANE Select
|
ENSP00000364831.5:p.Gly592Ala
|
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ENST00000375667.7:c.1268G>C
|
ENSP00000364819.3:p.Gly423Ala
|
|
ENST00000375679.8:c.1775G>C
|
ENSP00000364831.4:p.Gly592Ala
|
|
ENST00000431772.1:c.242G>C
|
ENSP00000389344.1:p.Gly81Ala
|
|
ENST00000619181.4:c.1294-1734G>C
|
ENSP00000483866.1:n.1294-1734G>C
|
|
NM_000085.4:c.1775G>C
|
NP_000076.2:p.Gly592Ala
|
|
NM_001165945.2:c.1268G>C
|
NP_001159417.2:p.Gly423Ala
|
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XM_011540619.1:c.1616G>C
|
XP_011538921.1:p.Gly539Ala
|
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XM_011540621.1:c.1124G>C
|
XP_011538923.1:p.Gly375Ala
|
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NM_000085.5:c.1775G>C
MANE Select
|
NP_000076.2:p.Gly592Ala
|
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