ENST00000224721.12:c.8311G=
MANE Select
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ENSP00000224721.9:p.Gly2771=
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ENST00000642965.1:c.2244G=
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ENSP00000495222.1:n.2244G=
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ENST00000647092.1:c.1908G=
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ENSP00000495176.1:n.1908G=
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ENST00000224721.10:c.8326G=
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ENSP00000224721.8:p.Gly2776=
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ENST00000398788.4:c.1591G=
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ENSP00000381768.3:p.Gly531=
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ENST00000475158.1:n.1847G=
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|
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ENST00000619887.4:c.1591G=
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ENSP00000478374.1:p.Gly531=
|
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ENST00000622827.4:c.8311G=
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ENSP00000483211.1:p.Gly2771=
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|
NM_001171933.1:c.1591G=
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NP_001165404.1:p.Gly531=
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NM_001171934.1:c.1591G=
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NP_001165405.1:p.Gly531=
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|
NM_022124.5:c.8311G=
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NP_071407.4:p.Gly2771=
|
|
XM_006717940.2:c.8506G=
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XP_006718003.1:p.Gly2836=
|
|
XM_006717942.2:c.8440G=
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XP_006718005.1:p.Gly2814=
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XM_011540039.1:c.8503G=
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XP_011538341.1:p.Gly2835=
|
|
XM_011540040.1:c.8500G=
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XP_011538342.1:p.Gly2834=
|
|
XM_011540041.1:c.8446G=
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XP_011538343.1:p.Gly2816=
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XM_011540042.1:c.8416G=
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XP_011538344.1:p.Gly2806=
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XM_011540043.1:c.8506G=
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XP_011538345.1:p.Gly2836=
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|
XM_011540044.1:c.8371G=
|
XP_011538346.1:p.Gly2791=
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|
XM_011540045.1:c.8506G=
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XP_011538347.1:p.Gly2836=
|
|
XM_011540046.1:c.7966G=
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XP_011538348.1:p.Gly2656=
|
|
XM_011540047.1:c.7324G=
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XP_011538349.1:p.Gly2442=
|
|
XM_011540052.1:c.4834G=
|
XP_011538354.1:p.Gly1612=
|
|
NM_022124.6:c.8311G=
MANE Select
|
NP_071407.4:p.Gly2771=
|
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