ENST00000355943.8:c.716G>A
MANE Select
|
ENSP00000348211.3:p.Cys239Tyr
|
|
ENST00000355943.7:c.716G>A
|
ENSP00000348211.3:p.Cys239Tyr
|
|
ENST00000447245.6:c.679-206G>A
|
ENSP00000399717.2:n.679-206G>A
|
|
ENST00000502462.6:n.1032G>A
|
|
|
ENST00000504098.1:c.278G>A
|
ENSP00000425708.1:p.Cys93Tyr
|
|
ENST00000509432.1:c.77G>A
|
ENSP00000426604.1:p.Cys26Tyr
|
|
ENST00000513706.2:n.2316G>A
|
|
|
ENST00000513807.5:c.230G>A
|
ENSP00000421134.1:p.Cys77Tyr
|
|
NM_001303249.1:c.679-206G>A
|
NP_001290178.1:n.679-206G>A
|
|
NM_001303250.1:c.443G>A
|
NP_001290179.1:p.Cys148Tyr
|
|
NM_138773.2:c.716G>A
|
NP_620128.1:p.Cys239Tyr
|
|
NM_001303249.2:c.679-206G>A
|
NP_001290178.1:n.679-206G>A
|
|
NM_001303250.2:c.443G>A
|
NP_001290179.1:p.Cys148Tyr
|
|
NM_138773.3:c.716G>A
|
NP_620128.1:p.Cys239Tyr
|
|
NR_138151.1:n.990G>A
|
|
|
NM_138773.4:c.716G>A
MANE Select
|
NP_620128.1:p.Cys239Tyr
|
|
NM_001303249.3:c.679-206G>A
|
NP_001290178.1:n.679-206G>A
|
|
NM_001303250.3:c.443G>A
|
NP_001290179.1:p.Cys148Tyr
|
|
NR_138151.2:n.955G>A
|
|
|