ENST00000622290.5:c.*374A>T
|
ENSP00000483331.2:n.*374A>T
|
|
ENST00000205557.12:c.4202A>T
MANE Select
|
ENSP00000205557.7:p.Asp1401Val
|
|
ENST00000640696.1:c.1016A>T
|
ENSP00000492197.1:p.Asp339Val
|
|
ENST00000205557.11:c.4202A>T
|
ENSP00000205557.7:p.Asp1401Val
|
|
ENST00000456970.6:c.3827A>T
|
ENSP00000405002.2:n.3827A>T
|
|
ENST00000576204.5:n.1065A>T
|
|
|
ENST00000622290.4:c.*1411A>T
|
ENSP00000483331.1:n.*1411A>T
|
|
NM_001171.5:c.4202A>T
|
NP_001162.4:p.Asp1401Val
|
|
XM_011522479.1:c.4169A>T
|
XP_011520781.1:p.Asp1390Val
|
|
XM_011522480.1:c.3860A>T
|
XP_011520782.1:p.Asp1287Val
|
|
XM_011522481.1:c.3860A>T
|
XP_011520783.1:p.Asp1287Val
|
|
XR_933134.1:n.539-5147T>A
|
|
|
NM_001351800.1:c.3860A>T
|
NP_001338729.1:p.Asp1287Val
|
|
NR_147784.1:n.3864A>T
|
|
|
XM_011522479.2:c.4169A>T
|
XP_011520781.1:p.Asp1390Val
|
|
XM_011522481.3:c.3860A>T
|
XP_011520783.1:p.Asp1287Val
|
|
XM_017023212.1:c.4034A>T
|
XP_016878701.1:p.Asp1345Val
|
|
XM_024450261.1:c.4238A>T
|
XP_024306029.1:p.Asp1413Val
|
|
NM_001171.6:c.4202A>T
MANE Select
|
NP_001162.5:p.Asp1401Val
|
|