ENST00000330062.8:c.588C=
MANE Select
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ENSP00000331897.4:p.Phe196=
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ENST00000330062.7:c.588C=
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ENSP00000331897.3:p.Phe196=
|
|
ENST00000540499.2:c.432C=
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ENSP00000446147.2:p.Phe144=
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ENST00000559482.5:c.261C=
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ENSP00000453016.1:p.Phe87=
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ENST00000560061.1:c.*213C=
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ENSP00000453254.1:n.*213C=
|
|
NM_001289910.1:c.432C= , LRG_611t1:c.432C=
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NP_001276839.1:p.Phe144=
|
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NM_001290114.1:c.198C=
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NP_001277043.1:p.Phe66=
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NM_002168.3:c.588C= , LRG_611t2:c.588C=
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NP_002159.2:p.Phe196=
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NM_001290114.2:c.198C=
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NP_001277043.1:p.Phe66=
|
|
NM_002168.4:c.588C=
MANE Select
|
NP_002159.2:p.Phe196=
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