ENST00000326828.6:c.665A>C
MANE Select
|
ENSP00000315602.5:p.Asn222Thr
|
|
ENST00000326828.5:c.665A>C
|
ENSP00000315602.5:p.Asn222Thr
|
|
ENST00000348639.7:c.665A>C
|
ENSP00000267951.4:p.Asn222Thr
|
|
ENST00000558903.1:n.372A>C
|
|
|
ENST00000559658.5:c.665A>C
|
ENSP00000452896.1:p.Asn222Thr
|
|
NM_000743.4:c.665A>C
|
NP_000734.2:p.Asn222Thr
|
|
NM_001166694.1:c.665A>C
|
NP_001160166.1:p.Asn222Thr
|
|
NR_046313.1:n.1166A>C
|
|
|
XM_006720382.1:c.464A>C
|
XP_006720445.1:p.Asn155Thr
|
|
XM_011521173.1:c.584A>C
|
XP_011519475.1:p.Asn195Thr
|
|
XM_006720382.3:c.464A>C
|
XP_006720445.1:p.Asn155Thr
|
|
NM_000743.5:c.665A>C
MANE Select
|
NP_000734.2:p.Asn222Thr
|
|
NM_001166694.2:c.665A>C
|
NP_001160166.1:p.Asn222Thr
|
|
NR_046313.2:n.867A>C
|
|
|