ENST00000330062.8:c.512G>C
MANE Select
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ENSP00000331897.4:p.Gly171Ala
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ENST00000330062.7:c.512G>C
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ENSP00000331897.3:p.Gly171Ala
|
|
ENST00000540499.2:c.356G>C
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ENSP00000446147.2:p.Gly119Ala
|
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ENST00000559482.5:c.208-107G>C
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ENSP00000453016.1:n.208-107G>C
|
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ENST00000560061.1:c.*137G>C
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ENSP00000453254.1:n.*137G>C
|
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NM_001289910.1:c.356G>C , LRG_611t1:c.356G>C
|
NP_001276839.1:p.Gly119Ala
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NM_001290114.1:c.122G>C
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NP_001277043.1:p.Gly41Ala
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NM_002168.3:c.512G>C , LRG_611t2:c.512G>C
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NP_002159.2:p.Gly171Ala
|
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NM_001290114.2:c.122G>C
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NP_001277043.1:p.Gly41Ala
|
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NM_002168.4:c.512G>C
MANE Select
|
NP_002159.2:p.Gly171Ala
|
|