ENST00000355943.8:c.756G>C
MANE Select
|
ENSP00000348211.3:p.Val252=
|
|
ENST00000355943.7:c.756G>C
|
ENSP00000348211.3:p.Val252=
|
|
ENST00000447245.6:c.679-166G>C
|
ENSP00000399717.2:n.679-166G>C
|
|
ENST00000502462.6:n.1072G>C
|
|
|
ENST00000504098.1:c.318G>C
|
ENSP00000425708.1:p.Val106=
|
|
ENST00000509432.1:c.117G>C
|
ENSP00000426604.1:p.Val39=
|
|
ENST00000513706.2:n.2356G>C
|
|
|
ENST00000513807.5:c.270G>C
|
ENSP00000421134.1:p.Val90=
|
|
NM_001303249.1:c.679-166G>C
|
NP_001290178.1:n.679-166G>C
|
|
NM_001303250.1:c.483G>C
|
NP_001290179.1:p.Val161=
|
|
NM_138773.2:c.756G>C
|
NP_620128.1:p.Val252=
|
|
NM_001303249.2:c.679-166G>C
|
NP_001290178.1:n.679-166G>C
|
|
NM_001303250.2:c.483G>C
|
NP_001290179.1:p.Val161=
|
|
NM_138773.3:c.756G>C
|
NP_620128.1:p.Val252=
|
|
NR_138151.1:n.1030G>C
|
|
|
NM_138773.4:c.756G>C
MANE Select
|
NP_620128.1:p.Val252=
|
|
NM_001303249.3:c.679-166G>C
|
NP_001290178.1:n.679-166G>C
|
|
NM_001303250.3:c.483G>C
|
NP_001290179.1:p.Val161=
|
|
NR_138151.2:n.995G>C
|
|
|