ENST00000224140.6:c.7699G>A
MANE Select
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ENSP00000224140.5:p.Gly2567Arg
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ENST00000224140.5:c.7699G>A
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ENSP00000224140.5:p.Gly2567Arg
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ENST00000436441.5:c.2512G>A
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ENSP00000409143.1:p.Gly838Arg
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ENST00000477049.1:n.849G>A
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NM_015046.5:c.7699G>A , LRG_268t1:c.7699G>A
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NP_055861.3:p.Gly2567Arg
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XM_005272171.1:c.7786G>A
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XP_005272228.1:p.Gly2596Arg
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XM_005272172.1:c.7786G>A
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XP_005272229.1:p.Gly2596Arg
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XM_005272173.1:c.7786G>A
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XP_005272230.1:p.Gly2596Arg
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XM_011518404.1:c.7786G>A
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XP_011516706.1:p.Gly2596Arg
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XM_011518405.1:c.7786G>A
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XP_011516707.1:p.Gly2596Arg
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XR_929739.1:n.7615G>A
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|
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NM_001351527.1:c.7699G>A
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NP_001338456.1:p.Gly2567Arg
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NM_001351528.1:c.7786G>A
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NP_001338457.1:p.Gly2596Arg
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NM_015046.6:c.7699G>A
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NP_055861.3:p.Gly2567Arg
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XM_005272172.3:c.7786G>A
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XP_005272229.1:p.Gly2596Arg
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XM_005272173.3:c.7786G>A
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XP_005272230.1:p.Gly2596Arg
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XM_011518404.3:c.7786G>A
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XP_011516706.1:p.Gly2596Arg
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XM_011518405.3:c.7786G>A
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XP_011516707.1:p.Gly2596Arg
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XM_017014496.1:c.2239G>A
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XP_016869985.1:p.Gly747Arg
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XR_001746251.1:n.7254G>A
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XR_929739.2:n.7615G>A
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NM_015046.7:c.7699G>A
MANE Select
|
NP_055861.3:p.Gly2567Arg
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NM_001351528.2:c.7786G>A
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NP_001338457.1:p.Gly2596Arg
|
|
NM_001351527.2:c.7699G>A
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NP_001338456.1:p.Gly2567Arg
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