ENST00000304611.13:c.1340C>A
MANE Select
|
ENSP00000303511.8:p.Ala447Asp
|
|
ENST00000244546.4:c.1340C>A
|
ENSP00000244546.4:p.Ala447Asp
|
|
ENST00000304611.12:c.1340C>A
|
ENSP00000303511.8:p.Ala447Asp
|
|
NM_000287.3:c.1340C>A
|
NP_000278.3:p.Ala447Asp
|
|
NM_001316313.1:c.1076C>A
|
NP_001303242.1:p.Ala359Asp
|
|
NR_133009.1:n.1433C>A
|
|
|
XM_011514661.1:c.1256C>A
|
XP_011512963.1:p.Ala419Asp
|
|
XR_926246.1:n.1433C>A
|
|
|
XM_011514661.2:c.1256C>A
|
XP_011512963.1:p.Ala419Asp
|
|
XR_001743466.2:n.2414C>A
|
|
|
NM_000287.4:c.1340C>A
MANE Select
|
NP_000278.3:p.Ala447Asp
|
|
NM_001316313.2:c.1076C>A
|
NP_001303242.1:p.Ala359Asp
|
|
NR_133009.2:n.1371C>A
|
|
|