ENST00000348974.5:c.818T>G
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ENSP00000330021.7:p.Phe273Cys
|
|
ENST00000394236.9:c.818T>G
MANE Select
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ENSP00000377783.3:p.Phe273Cys
|
|
ENST00000407433.6:c.773T>G
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ENSP00000385794.2:p.Phe258Cys
|
|
ENST00000647936.1:c.818T>G
|
ENSP00000496822.1:p.Phe273Cys
|
|
ENST00000648381.1:n.986T>G
|
|
|
ENST00000648853.1:c.776T>G
|
ENSP00000497262.1:p.Phe259Cys
|
|
ENST00000649103.1:c.917T>G
|
ENSP00000497962.1:n.917T>G
|
|
ENST00000650591.1:c.914T>G
|
ENSP00000497376.1:p.Phe305Cys
|
|
ENST00000394236.7:c.818T>G
|
ENSP00000377783.3:p.Phe273Cys
|
|
ENST00000407433.5:c.425T>G
|
ENSP00000385794.1:p.Phe142Cys
|
|
NM_000313.3:c.818T>G , LRG_572t1:c.818T>G
|
NP_000304.2:p.Phe273Cys
|
|
NM_001314077.1:c.914T>G , LRG_572t2:c.914T>G
|
NP_001301006.1:p.Phe305Cys
|
|
NM_000313.4:c.818T>G
MANE Select
|
NP_000304.2:p.Phe273Cys
|
|
NM_001314077.2:c.914T>G
|
NP_001301006.1:p.Phe305Cys
|
|