ENST00000405440.7:c.487A>C
MANE Select
|
ENSP00000384152.3:p.Asn163His
|
|
ENST00000310346.8:c.487A>C
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ENSP00000309913.4:p.Asn163His
|
|
ENST00000349716.9:c.337A>C
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ENSP00000337723.5:p.Asn113His
|
|
ENST00000405440.6:c.487A>C
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ENSP00000384152.2:p.Asn163His
|
|
ENST00000526441.1:c.487A>C
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ENSP00000433292.1:p.Asn163His
|
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ENST00000552726.1:n.538A>C
|
|
|
NM_000192.3:c.487A>C , LRG_670t1:c.487A>C
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NP_000183.2:p.Asn163His
|
|
NM_080717.2:c.337A>C
|
NP_542448.1:p.Asn113His
|
|
NM_181486.2:c.487A>C
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NP_852259.1:p.Asn163His
|
|
XM_017019912.1:c.535A>C
|
XP_016875401.1:p.Asn179His
|
|
NM_080717.3:c.337A>C
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NP_542448.1:p.Asn113His
|
|
NM_181486.4:c.487A>C
MANE Select
|
NP_852259.1:p.Asn163His
|
|
NM_080717.4:c.337A>C
|
NP_542448.1:p.Asn113His
|
|