ENST00000029410.10:c.779A>T
MANE Select
|
ENSP00000029410.5:p.Asp260Val
|
|
ENST00000029410.9:c.779A>T
|
ENSP00000029410.5:p.Asp260Val
|
|
ENST00000505145.1:n.1877A>T
|
|
|
ENST00000505433.5:c.*285A>T
|
ENSP00000425591.1:n.*285A>T
|
|
ENST00000515353.1:n.1601A>T
|
|
|
NM_007255.2:c.779A>T
|
NP_009186.1:p.Asp260Val
|
|
XM_005265805.2:c.437A>T
|
XP_005265862.1:p.Asp146Val
|
|
XM_006714816.2:c.299A>T
|
XP_006714879.1:p.Asp100Val
|
|
XM_011534421.1:c.437A>T
|
XP_011532723.1:p.Asp146Val
|
|
XM_006714816.4:c.299A>T
|
XP_006714879.1:p.Asp100Val
|
|
XM_017008999.2:c.437A>T
|
XP_016864488.1:p.Asp146Val
|
|
NM_007255.3:c.779A>T
MANE Select
|
NP_009186.1:p.Asp260Val
|
|