ENST00000292408.9:c.2281T>G
MANE Select
|
ENSP00000292408.4:p.Phe761Val
|
|
ENST00000292408.8:c.2281T>G
|
ENSP00000292408.4:p.Phe761Val
|
|
ENST00000393637.5:c.2161T>G
|
ENSP00000377254.1:p.Phe721Val
|
|
ENST00000393648.6:c.2077T>G
|
ENSP00000377259.2:p.Phe693Val
|
|
ENST00000502906.5:c.2281T>G
|
ENSP00000424960.1:p.Phe761Val
|
|
ENST00000513423.1:n.229T>G
|
|
|
NM_001291980.1:c.2077T>G
|
NP_001278909.1:p.Phe693Val
|
|
NM_002011.4:c.2281T>G
|
NP_002002.3:p.Phe761Val
|
|
NM_022963.3:c.2161T>G
|
NP_075252.2:p.Phe721Val
|
|
NM_213647.2:c.2281T>G
|
NP_998812.1:p.Phe761Val
|
|
XM_005265838.2:c.2281T>G
|
XP_005265895.1:p.Phe761Val
|
|
XM_011534464.1:c.2374T>G
|
XP_011532766.1:p.Phe792Val
|
|
XM_011534465.1:c.1963T>G
|
XP_011532767.1:p.Phe655Val
|
|
NM_001354984.1:c.2281T>G
|
NP_001341913.1:p.Phe761Val
|
|
NM_213647.3:c.2281T>G
MANE Select
|
NP_998812.1:p.Phe761Val
|
|
NM_001291980.2:c.2077T>G
|
NP_001278909.1:p.Phe693Val
|
|
NM_001354984.2:c.2281T>G
|
NP_001341913.1:p.Phe761Val
|
|
NM_002011.5:c.2281T>G
|
NP_002002.3:p.Phe761Val
|
|