ENST00000355943.8:c.729A>T
MANE Select
|
ENSP00000348211.3:p.Gly243=
|
|
ENST00000355943.7:c.729A>T
|
ENSP00000348211.3:p.Gly243=
|
|
ENST00000447245.6:c.679-193A>T
|
ENSP00000399717.2:n.679-193A>T
|
|
ENST00000502462.6:n.1045A>T
|
|
|
ENST00000504098.1:c.291A>T
|
ENSP00000425708.1:p.Gly97=
|
|
ENST00000509432.1:c.90A>T
|
ENSP00000426604.1:p.Gly30=
|
|
ENST00000513706.2:n.2329A>T
|
|
|
ENST00000513807.5:c.243A>T
|
ENSP00000421134.1:p.Gly81=
|
|
NM_001303249.1:c.679-193A>T
|
NP_001290178.1:n.679-193A>T
|
|
NM_001303250.1:c.456A>T
|
NP_001290179.1:p.Gly152=
|
|
NM_138773.2:c.729A>T
|
NP_620128.1:p.Gly243=
|
|
NM_001303249.2:c.679-193A>T
|
NP_001290178.1:n.679-193A>T
|
|
NM_001303250.2:c.456A>T
|
NP_001290179.1:p.Gly152=
|
|
NM_138773.3:c.729A>T
|
NP_620128.1:p.Gly243=
|
|
NR_138151.1:n.1003A>T
|
|
|
NM_138773.4:c.729A>T
MANE Select
|
NP_620128.1:p.Gly243=
|
|
NM_001303249.3:c.679-193A>T
|
NP_001290178.1:n.679-193A>T
|
|
NM_001303250.3:c.456A>T
|
NP_001290179.1:p.Gly152=
|
|
NR_138151.2:n.968A>T
|
|
|