ENST00000682617.1:c.2621C>T
|
ENSP00000507912.1:p.Ala874Val
|
|
ENST00000683962.1:c.*2177C>T
|
ENSP00000506854.1:n.*2177C>T
|
|
ENST00000311895.8:c.2483C>T
MANE Select
|
ENSP00000310520.7:p.Ala828Val
|
|
ENST00000311895.7:c.2483C>T
|
ENSP00000310520.7:p.Ala828Val
|
|
ENST00000389138.7:n.1760C>T
|
|
|
NM_005236.2:c.2483C>T , LRG_463t1:c.2483C>T
|
NP_005227.1:p.Ala828Val
|
|
XM_011522424.1:c.2621C>T
|
XP_011520726.1:p.Ala874Val
|
|
XM_011522425.1:c.1940C>T
|
XP_011520727.1:p.Ala647Val
|
|
XM_011522426.1:c.1694C>T
|
XP_011520728.1:p.Ala565Val
|
|
XM_011522427.1:c.1133C>T
|
XP_011520729.1:p.Ala378Val
|
|
XR_932805.1:n.2642C>T
|
|
|
XM_011522424.3:c.2621C>T
|
XP_011520726.1:p.Ala874Val
|
|
XM_017023043.2:c.1694C>T
|
XP_016878532.1:p.Ala565Val
|
|
NM_005236.3:c.2483C>T
MANE Select
|
NP_005227.1:p.Ala828Val
|
|