ENST00000302068.9:c.1238A>T
MANE Select
|
ENSP00000306099.4:p.Asp413Val
|
|
ENST00000302068.8:c.1238A>T
|
ENSP00000306099.4:p.Asp413Val
|
|
ENST00000502545.5:n.939+486A>T
|
|
|
ENST00000509493.1:c.581A>T
|
ENSP00000426757.1:p.Asp194Val
|
|
NM_001184741.1:c.1061A>T
|
NP_001171670.1:p.Asp354Val
|
|
NM_005141.4:c.1238A>T , LRG_558t1:c.1238A>T
|
NP_005132.2:p.Asp413Val
|
|
NM_001382759.1:c.1106A>T
|
NP_001369688.1:p.Asp369Val
|
|
NM_001382760.1:c.1238A>T
|
NP_001369689.1:p.Asp413Val
|
|
NM_001382761.1:c.1238A>T
|
NP_001369690.1:p.Asp413Val
|
|
NM_001382762.1:c.938A>T
|
NP_001369691.1:p.Asp313Val
|
|
NM_001382763.1:c.1229A>T
|
NP_001369692.1:p.Asp410Val
|
|
NM_001382764.1:c.*12A>T
|
NP_001369693.1:n.*12A>T
|
|
NM_001382765.1:c.1220+18A>T
|
NP_001369694.1:n.1220+18A>T
|
|
NM_005141.5:c.1238A>T
MANE Select
|
NP_005132.2:p.Asp413Val
|
|