ENST00000215882.10:c.556G>T
MANE Select
|
ENSP00000215882.5:p.Ala186Ser
|
|
ENST00000215882.9:c.556G>T
|
ENSP00000215882.5:p.Ala186Ser
|
|
ENST00000451283.5:c.247G>T
|
ENSP00000401480.1:p.Ala83Ser
|
|
ENST00000461267.1:n.702G>T
|
|
|
ENST00000470922.5:n.698G>T
|
|
|
NM_001256534.1:c.577G>T
|
NP_001243463.1:p.Ala193Ser
|
|
NM_001287387.1:c.247G>T
|
NP_001274316.1:p.Ala83Ser
|
|
NM_005984.4:c.556G>T
|
NP_005975.1:p.Ala186Ser
|
|
NR_046298.2:n.607G>T
|
|
|
NM_005984.5:c.556G>T
MANE Select
|
NP_005975.1:p.Ala186Ser
|
|
NM_001256534.2:c.577G>T
|
NP_001243463.1:p.Ala193Ser
|
|
NM_001287387.2:c.247G>T
|
NP_001274316.1:p.Ala83Ser
|
|
NR_046298.3:n.480G>T
|
|
|