ENST00000541562.6:c.2367T>G
|
ENSP00000441000.2:p.Ala789=
|
|
ENST00000672801.1:c.2361T>G
|
ENSP00000500615.1:p.Ala787=
|
|
ENST00000676266.1:c.2367T>G
MANE Select
|
ENSP00000502585.1:p.Ala789=
|
|
ENST00000321897.9:c.2367T>G
|
ENSP00000316092.5:p.Ala789=
|
|
ENST00000469358.5:n.2355T>G
|
|
|
ENST00000473916.1:n.78T>G
|
|
|
ENST00000476162.5:n.1154T>G
|
|
|
ENST00000477052.1:n.453T>G
|
|
|
ENST00000477288.5:n.4980T>G
|
|
|
ENST00000541562.5:c.2457T>G
|
ENSP00000441000.1:p.Ala819=
|
|
ENST00000542001.5:c.2361T>G
|
ENSP00000438200.2:p.Ala787=
|
|
ENST00000625423.2:c.1947T>G
|
ENSP00000485818.1:p.Ala649=
|
|
NM_001167733.2:c.1947T>G
|
NP_001161205.1:p.Ala649=
|
|
NM_001167734.1:c.2457T>G
|
NP_001161206.1:p.Ala819=
|
|
NM_020442.5:c.2367T>G
|
NP_065175.4:p.Ala789=
|
|
NM_001167733.3:c.1947T>G
|
NP_001161205.1:p.Ala649=
|
|
NM_001167734.2:c.2457T>G
|
NP_001161206.1:p.Ala819=
|
|
NM_020442.6:c.2367T>G
MANE Select
|
NP_065175.4:p.Ala789=
|
|