ENST00000327047.6:c.508A>C
MANE Select
|
ENSP00000322280.1:p.Asn170His
|
|
ENST00000468836.2:c.656A>C
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ENSP00000419892.2:n.656A>C
|
|
ENST00000295911.6:c.280A>C
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ENSP00000295911.2:p.Asn94His
|
|
ENST00000327047.5:c.508A>C
|
ENSP00000322280.1:p.Asn170His
|
|
ENST00000328863.8:c.547A>C
|
ENSP00000329158.4:p.Asn183His
|
|
ENST00000468836.1:c.280A>C
|
ENSP00000419892.1:p.Asn94His
|
|
ENST00000562308.5:c.104+13455A>C
|
|
|
ENST00000565169.1:c.162+13455A>C
|
|
|
ENST00000569170.5:c.162+13455A>C
|
|
|
NM_001195794.1:c.547A>C , LRG_700t1:c.547A>C
|
NP_001182723.1:p.Asn183His
|
|
NM_001256819.1:c.*122A>C
|
NP_001243748.1:n.*122A>C
|
|
NM_052995.2:c.280A>C , LRG_700t2:c.280A>C
|
NP_443721.1:p.Asn94His
|
|
NM_174878.2:c.508A>C
|
NP_777367.1:p.Asn170His
|
|
NR_046380.2:n.989A>C
|
|
|
XR_924167.1:n.820A>C
|
|
|
NM_001256819.2:c.*122A>C
|
NP_001243748.1:n.*122A>C
|
|
NM_174878.3:c.508A>C
MANE Select
|
NP_777367.1:p.Asn170His
|
|
NR_046380.3:n.717A>C
|
|
|