ENST00000330062.8:c.508A>G
MANE Select
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ENSP00000331897.4:p.Ile170Val
|
|
ENST00000330062.7:c.508A>G
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ENSP00000331897.3:p.Ile170Val
|
|
ENST00000540499.2:c.352A>G
|
ENSP00000446147.2:p.Ile118Val
|
|
ENST00000559482.5:c.208-111A>G
|
ENSP00000453016.1:n.208-111A>G
|
|
ENST00000560061.1:c.*133A>G
|
ENSP00000453254.1:n.*133A>G
|
|
NM_001289910.1:c.352A>G , LRG_611t1:c.352A>G
|
NP_001276839.1:p.Ile118Val
|
|
NM_001290114.1:c.118A>G
|
NP_001277043.1:p.Ile40Val
|
|
NM_002168.3:c.508A>G , LRG_611t2:c.508A>G
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NP_002159.2:p.Ile170Val
|
|
NM_001290114.2:c.118A>G
|
NP_001277043.1:p.Ile40Val
|
|
NM_002168.4:c.508A>G
MANE Select
|
NP_002159.2:p.Ile170Val
|
|