ENST00000355943.8:c.1215T>C
MANE Select
|
ENSP00000348211.3:p.Ile405=
|
|
ENST00000355943.7:c.1215T>C
|
ENSP00000348211.3:p.Ile405=
|
|
ENST00000447245.6:c.972T>C
|
ENSP00000399717.2:p.Ile324=
|
|
ENST00000504098.1:c.777T>C
|
ENSP00000425708.1:p.Ile259=
|
|
ENST00000509432.1:c.576T>C
|
ENSP00000426604.1:p.Ile192=
|
|
ENST00000513706.2:n.2815T>C
|
|
|
ENST00000513807.5:c.729T>C
|
ENSP00000421134.1:p.Ile243=
|
|
NM_001303249.1:c.972T>C
|
NP_001290178.1:p.Ile324=
|
|
NM_001303250.1:c.942T>C
|
NP_001290179.1:p.Ile314=
|
|
NM_138773.2:c.1215T>C
|
NP_620128.1:p.Ile405=
|
|
NM_001303249.2:c.972T>C
|
NP_001290178.1:p.Ile324=
|
|
NM_001303250.2:c.942T>C
|
NP_001290179.1:p.Ile314=
|
|
NM_138773.3:c.1215T>C
|
NP_620128.1:p.Ile405=
|
|
NR_138151.1:n.1489T>C
|
|
|
NM_138773.4:c.1215T>C
MANE Select
|
NP_620128.1:p.Ile405=
|
|
NM_001303249.3:c.972T>C
|
NP_001290178.1:p.Ile324=
|
|
NM_001303250.3:c.942T>C
|
NP_001290179.1:p.Ile314=
|
|
NR_138151.2:n.1454T>C
|
|
|