ENST00000456935.7:c.674A>T
MANE Select
|
ENSP00000395473.2:p.Asp225Val
|
|
ENST00000221363.8:c.674A>T
|
ENSP00000221363.4:p.Asp225Val
|
|
ENST00000456935.6:c.674A>T
|
ENSP00000395473.2:p.Asp225Val
|
|
ENST00000466794.5:n.656A>T
|
|
|
ENST00000486847.2:c.377A>T
|
ENSP00000470174.1:p.Asp126Val
|
|
NM_000528.3:c.674A>T
|
NP_000519.2:p.Asp225Val
|
|
NM_001173498.1:c.674A>T
|
NP_001166969.1:p.Asp225Val
|
|
XM_005259913.1:c.674A>T
|
XP_005259970.1:p.Asp225Val
|
|
XM_005259913.2:c.674A>T
|
XP_005259970.1:p.Asp225Val
|
|
XM_024451518.1:c.-345A>T
|
XP_024307286.1:n.-345A>T
|
|
NM_000528.4:c.674A>T
MANE Select
|
NP_000519.2:p.Asp225Val
|
|
NM_001173498.2:c.674A>T
|
NP_001166969.1:p.Asp225Val
|
|