ENST00000700075.1:c.8G>C
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ENSP00000514784.1:p.Gly3Ala
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ENST00000342771.10:c.1940G>C
MANE Select
|
ENSP00000344087.4:p.Gly647Ala
|
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ENST00000439256.2:c.38G>C
|
ENSP00000407058.2:p.Gly13Ala
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ENST00000443672.2:c.275G>C
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ENSP00000393548.2:p.Gly92Ala
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ENST00000449547.6:c.33G>C
|
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ENST00000464768.2:n.608G>C
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ENST00000644359.1:c.521G>C
|
ENSP00000494561.1:p.Gly174Ala
|
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ENST00000644506.1:c.566G>C
|
ENSP00000496672.1:p.Gly189Ala
|
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ENST00000644939.1:c.1937G>C
|
ENSP00000496726.1:p.Gly646Ala
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ENST00000644949.1:c.271G>C
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ENST00000646136.1:n.251G>C
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ENST00000647140.1:c.805G>C
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ENST00000342771.8:c.1940G>C
|
ENSP00000344087.4:p.Gly647Ala
|
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ENST00000406775.6:c.1868G>C
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ENSP00000385263.2:p.Gly623Ala
|
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ENST00000439256.1:c.38G>C
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|
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ENST00000443672.1:c.520G>C
|
|
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ENST00000464768.1:n.606G>C
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ENST00000465899.1:n.437G>C
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|
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ENST00000498384.5:n.308G>C
|
|
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ENST00000611706.4:c.1196G>C
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ENSP00000478134.1:p.Gly399Ala
|
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ENST00000615871.4:c.1124G>C
|
ENSP00000479325.1:p.Gly375Ala
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NM_001127231.2:c.1868G>C
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NP_001120703.1:p.Gly623Ala
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NM_015570.3:c.1940G>C
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NP_056385.1:p.Gly647Ala
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XM_005250257.1:c.587G>C
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XP_005250314.1:p.Gly196Ala
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XM_011516010.1:c.1961G>C
|
XP_011514312.1:p.Gly654Ala
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XM_011516011.1:c.1958G>C
|
XP_011514313.1:p.Gly653Ala
|
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XM_011516012.1:c.1895G>C
|
XP_011514314.1:p.Gly632Ala
|
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XM_011516013.1:c.1889G>C
|
XP_011514315.1:p.Gly630Ala
|
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XM_011516014.1:c.1859G>C
|
XP_011514316.1:p.Gly620Ala
|
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XM_011516015.1:c.1697G>C
|
XP_011514317.1:p.Gly566Ala
|
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XM_011516016.1:c.1670G>C
|
XP_011514318.1:p.Gly557Ala
|
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XM_011516017.1:c.1487G>C
|
XP_011514319.1:p.Gly496Ala
|
|
XM_011516018.1:c.1460G>C
|
XP_011514320.1:p.Gly487Ala
|
|
XM_005250257.2:c.587G>C
|
XP_005250314.1:p.Gly196Ala
|
|
XM_011516010.2:c.1961G>C
|
XP_011514312.1:p.Gly654Ala
|
|
XM_011516011.2:c.1958G>C
|
XP_011514313.1:p.Gly653Ala
|
|
XM_011516012.2:c.1895G>C
|
XP_011514314.1:p.Gly632Ala
|
|
XM_011516013.2:c.1889G>C
|
XP_011514315.1:p.Gly630Ala
|
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XM_011516014.2:c.1859G>C
|
XP_011514316.1:p.Gly620Ala
|
|
XM_011516017.2:c.1487G>C
|
XP_011514319.1:p.Gly496Ala
|
|
XM_011516018.2:c.1460G>C
|
XP_011514320.1:p.Gly487Ala
|
|
XM_017011951.2:c.1961G>C
|
XP_016867440.1:p.Gly654Ala
|
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NM_001127231.3:c.1868G>C
|
NP_001120703.1:p.Gly623Ala
|
|
NM_015570.4:c.1940G>C
MANE Select
|
NP_056385.1:p.Gly647Ala
|
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