ENST00000220616.9:c.8117A>C
MANE Select
|
ENSP00000220616.4:p.Asn2706Thr
|
|
ENST00000220616.8:c.8117A>C
|
ENSP00000220616.4:p.Asn2706Thr
|
|
ENST00000519178.5:c.3483A>C
|
|
|
ENST00000519543.5:c.2516A>C
|
ENSP00000430430.1:p.Asn839Thr
|
|
ENST00000521107.1:c.329A>C
|
ENSP00000430161.1:p.Asn110Thr
|
|
ENST00000522691.1:n.203A>C
|
|
|
ENST00000523756.5:c.4772A>C
|
|
|
NM_003235.4:c.8117A>C
|
NP_003226.4:p.Asn2706Thr
|
|
XM_005251038.3:c.7925A>C
|
XP_005251095.1:p.Asn2642Thr
|
|
XM_006716622.2:c.8054A>C
|
XP_006716685.1:p.Asn2685Thr
|
|
XM_005251038.4:c.7925A>C
|
XP_005251095.1:p.Asn2642Thr
|
|
XM_006716622.3:c.8054A>C
|
XP_006716685.1:p.Asn2685Thr
|
|
XM_017013793.1:c.8051A>C
|
XP_016869282.1:p.Asn2684Thr
|
|
XM_017013794.1:c.7982A>C
|
XP_016869283.1:p.Asn2661Thr
|
|
XM_017013795.1:c.7946A>C
|
XP_016869284.1:p.Asn2649Thr
|
|
XM_017013796.1:c.7898A>C
|
XP_016869285.1:p.Asn2633Thr
|
|
XM_017013797.1:c.7856A>C
|
XP_016869286.1:p.Asn2619Thr
|
|
NM_003235.5:c.8117A>C
MANE Select
|
NP_003226.4:p.Asn2706Thr
|
|