ENST00000220616.9:c.6743C>A
MANE Select
|
ENSP00000220616.4:p.Pro2248His
|
|
ENST00000220616.8:c.6743C>A
|
ENSP00000220616.4:p.Pro2248His
|
|
ENST00000518108.1:c.168+92C>A
|
|
|
ENST00000519178.5:c.2109C>A
|
|
|
ENST00000519543.5:c.1142C>A
|
ENSP00000430430.1:p.Pro381His
|
|
ENST00000522523.5:n.804C>A
|
|
|
ENST00000523756.5:c.3398C>A
|
|
|
NM_003235.4:c.6743C>A
|
NP_003226.4:p.Pro2248His
|
|
XM_005251038.3:c.6551C>A
|
XP_005251095.1:p.Pro2184His
|
|
XM_006716622.2:c.6680C>A
|
XP_006716685.1:p.Pro2227His
|
|
XM_005251038.4:c.6551C>A
|
XP_005251095.1:p.Pro2184His
|
|
XM_006716622.3:c.6680C>A
|
XP_006716685.1:p.Pro2227His
|
|
XM_017013793.1:c.6677C>A
|
XP_016869282.1:p.Pro2226His
|
|
XM_017013794.1:c.6743C>A
|
XP_016869283.1:p.Pro2248His
|
|
XM_017013795.1:c.6572C>A
|
XP_016869284.1:p.Pro2191His
|
|
XM_017013796.1:c.6524C>A
|
XP_016869285.1:p.Pro2175His
|
|
XM_017013797.1:c.6482C>A
|
XP_016869286.1:p.Pro2161His
|
|
XM_017013798.1:c.6743C>A
|
XP_016869287.1:p.Pro2248His
|
|
NM_003235.5:c.6743C>A
MANE Select
|
NP_003226.4:p.Pro2248His
|
|