ENST00000220616.9:c.8087A>C
MANE Select
|
ENSP00000220616.4:p.Asn2696Thr
|
|
ENST00000220616.8:c.8087A>C
|
ENSP00000220616.4:p.Asn2696Thr
|
|
ENST00000519178.5:c.3453A>C
|
|
|
ENST00000519543.5:c.2486A>C
|
ENSP00000430430.1:p.Asn829Thr
|
|
ENST00000521107.1:c.299A>C
|
ENSP00000430161.1:p.Asn100Thr
|
|
ENST00000522691.1:n.173A>C
|
|
|
ENST00000523756.5:c.4742A>C
|
|
|
NM_003235.4:c.8087A>C
|
NP_003226.4:p.Asn2696Thr
|
|
XM_005251038.3:c.7895A>C
|
XP_005251095.1:p.Asn2632Thr
|
|
XM_006716622.2:c.8024A>C
|
XP_006716685.1:p.Asn2675Thr
|
|
XM_005251038.4:c.7895A>C
|
XP_005251095.1:p.Asn2632Thr
|
|
XM_006716622.3:c.8024A>C
|
XP_006716685.1:p.Asn2675Thr
|
|
XM_017013793.1:c.8021A>C
|
XP_016869282.1:p.Asn2674Thr
|
|
XM_017013794.1:c.7952A>C
|
XP_016869283.1:p.Asn2651Thr
|
|
XM_017013795.1:c.7916A>C
|
XP_016869284.1:p.Asn2639Thr
|
|
XM_017013796.1:c.7868A>C
|
XP_016869285.1:p.Asn2623Thr
|
|
XM_017013797.1:c.7826A>C
|
XP_016869286.1:p.Asn2609Thr
|
|
NM_003235.5:c.8087A>C
MANE Select
|
NP_003226.4:p.Asn2696Thr
|
|