ENST00000330062.8:c.586T>G
MANE Select
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ENSP00000331897.4:p.Phe196Val
|
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ENST00000330062.7:c.586T>G
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ENSP00000331897.3:p.Phe196Val
|
|
ENST00000540499.2:c.430T>G
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ENSP00000446147.2:p.Phe144Val
|
|
ENST00000559482.5:c.259T>G
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ENSP00000453016.1:p.Phe87Val
|
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ENST00000560061.1:c.*211T>G
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ENSP00000453254.1:n.*211T>G
|
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NM_001289910.1:c.430T>G , LRG_611t1:c.430T>G
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NP_001276839.1:p.Phe144Val
|
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NM_001290114.1:c.196T>G
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NP_001277043.1:p.Phe66Val
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NM_002168.3:c.586T>G , LRG_611t2:c.586T>G
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NP_002159.2:p.Phe196Val
|
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NM_001290114.2:c.196T>G
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NP_001277043.1:p.Phe66Val
|
|
NM_002168.4:c.586T>G
MANE Select
|
NP_002159.2:p.Phe196Val
|
|