ENST00000261769.10:c.2078G>A
MANE Select
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ENSP00000261769.4:p.Gly693Asp
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ENST00000261769.9:c.2078G>A
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ENSP00000261769.4:p.Gly693Asp
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|
ENST00000422392.6:c.1895G>A
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ENSP00000414946.2:p.Gly632Asp
|
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ENST00000562118.1:n.296G>A
|
|
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ENST00000562836.5:n.2149G>A
|
|
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ENST00000566510.5:c.*744G>A
|
ENSP00000458139.1:n.*744G>A
|
|
ENST00000566612.5:c.*318G>A
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ENSP00000454782.1:n.*318G>A
|
|
ENST00000611625.4:c.2141G>A
|
ENSP00000481063.1:p.Gly714Asp
|
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ENST00000612417.4:c.1830+1421G>A
|
ENSP00000478360.1:n.1830+1421G>A
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ENST00000621016.4:c.1865+1386G>A
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ENSP00000480664.1:n.1865+1386G>A
|
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NM_004360.3:c.2078G>A , LRG_301t1:c.2078G>A
|
NP_004351.1:p.Gly693Asp
|
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XM_011523488.1:c.1343G>A
|
XP_011521790.1:p.Gly448Asp
|
|
XM_011523489.1:c.1343G>A
|
XP_011521791.1:p.Gly448Asp
|
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NM_001317184.1:c.1895G>A
|
NP_001304113.1:p.Gly632Asp
|
|
NM_001317185.1:c.530G>A
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NP_001304114.1:p.Gly177Asp
|
|
NM_001317186.1:c.113G>A
|
NP_001304115.1:p.Gly38Asp
|
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NM_004360.4:c.2078G>A
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NP_004351.1:p.Gly693Asp
|
|
NM_004360.5:c.2078G>A
MANE Select
|
NP_004351.1:p.Gly693Asp
|
|
NM_001317184.2:c.1895G>A
|
NP_001304113.1:p.Gly632Asp
|
|
NM_001317185.2:c.530G>A
|
NP_001304114.1:p.Gly177Asp
|
|
NM_001317186.2:c.113G>A
|
NP_001304115.1:p.Gly38Asp
|
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