ENST00000220616.9:c.8088C>T
MANE Select
|
ENSP00000220616.4:p.Asn2696=
|
|
ENST00000220616.8:c.8088C>T
|
ENSP00000220616.4:p.Asn2696=
|
|
ENST00000519178.5:c.3454C>T
|
|
|
ENST00000519543.5:c.2487C>T
|
ENSP00000430430.1:p.Asn829=
|
|
ENST00000521107.1:c.300C>T
|
ENSP00000430161.1:p.Asn100=
|
|
ENST00000522691.1:n.174C>T
|
|
|
ENST00000523756.5:c.4743C>T
|
|
|
NM_003235.4:c.8088C>T
|
NP_003226.4:p.Asn2696=
|
|
XM_005251038.3:c.7896C>T
|
XP_005251095.1:p.Asn2632=
|
|
XM_006716622.2:c.8025C>T
|
XP_006716685.1:p.Asn2675=
|
|
XM_005251038.4:c.7896C>T
|
XP_005251095.1:p.Asn2632=
|
|
XM_006716622.3:c.8025C>T
|
XP_006716685.1:p.Asn2675=
|
|
XM_017013793.1:c.8022C>T
|
XP_016869282.1:p.Asn2674=
|
|
XM_017013794.1:c.7953C>T
|
XP_016869283.1:p.Asn2651=
|
|
XM_017013795.1:c.7917C>T
|
XP_016869284.1:p.Asn2639=
|
|
XM_017013796.1:c.7869C>T
|
XP_016869285.1:p.Asn2623=
|
|
XM_017013797.1:c.7827C>T
|
XP_016869286.1:p.Asn2609=
|
|
NM_003235.5:c.8088C>T
MANE Select
|
NP_003226.4:p.Asn2696=
|
|