ENST00000456935.7:c.2084C>A
MANE Select
|
ENSP00000395473.2:p.Ala695Asp
|
|
ENST00000221363.8:c.2081C>A
|
ENSP00000221363.4:p.Ala694Asp
|
|
ENST00000456935.6:c.2084C>A
|
ENSP00000395473.2:p.Ala695Asp
|
|
ENST00000466794.5:n.2674C>A
|
|
|
NM_000528.3:c.2084C>A
|
NP_000519.2:p.Ala695Asp
|
|
NM_001173498.1:c.2081C>A
|
NP_001166969.1:p.Ala694Asp
|
|
XM_005259913.1:c.2087C>A
|
XP_005259970.1:p.Ala696Asp
|
|
XM_011528017.1:c.983C>A
|
XP_011526319.1:p.Ala328Asp
|
|
XM_005259913.2:c.2087C>A
|
XP_005259970.1:p.Ala696Asp
|
|
XM_024451518.1:c.983C>A
|
XP_024307286.1:p.Ala328Asp
|
|
NM_000528.4:c.2084C>A
MANE Select
|
NP_000519.2:p.Ala695Asp
|
|
NM_001173498.2:c.2081C>A
|
NP_001166969.1:p.Ala694Asp
|
|