ENST00000265594.9:c.1288T>G
MANE Select
|
ENSP00000265594.4:p.Tyr430Asp
|
|
ENST00000265594.8:c.1288T>G
|
ENSP00000265594.4:p.Tyr430Asp
|
|
ENST00000476176.5:c.1147T>G
|
ENSP00000420433.1:p.Tyr383Asp
|
|
ENST00000492597.5:c.961T>G
|
ENSP00000419898.1:p.Tyr321Asp
|
|
ENST00000495767.5:c.*869T>G
|
ENSP00000419658.1:n.*869T>G
|
|
ENST00000497830.5:c.*885T>G
|
ENSP00000420088.1:n.*885T>G
|
|
ENST00000497959.5:c.1174T>G
|
ENSP00000420648.1:p.Tyr392Asp
|
|
ENST00000539926.5:c.838T>G
|
ENSP00000441253.2:p.Tyr280Asp
|
|
ENST00000610757.4:c.838T>G
|
ENSP00000480435.1:p.Tyr280Asp
|
|
ENST00000629669.2:c.1174T>G
|
ENSP00000486824.1:p.Tyr392Asp
|
|
NM_001293273.1:c.937T>G
|
NP_001280202.1:p.Tyr313Asp
|
|
NM_020166.4:c.1288T>G
|
NP_064551.3:p.Tyr430Asp
|
|
NR_120639.1:n.1202T>G
|
|
|
NR_120640.1:n.1955T>G
|
|
|
XM_006713702.1:c.961T>G
|
XP_006713765.1:p.Tyr321Asp
|
|
XM_011512992.1:c.1174T>G
|
XP_011511294.1:p.Tyr392Asp
|
|
XM_011512993.1:c.1288T>G
|
XP_011511295.1:p.Tyr430Asp
|
|
XR_241502.2:n.1435T>G
|
|
|
XR_924159.1:n.1435T>G
|
|
|
NM_001363880.1:c.961T>G
|
NP_001350809.1:p.Tyr321Asp
|
|
XM_011512992.2:c.1174T>G
|
XP_011511294.1:p.Tyr392Asp
|
|
XR_001740207.2:n.1411T>G
|
|
|
XR_001740208.2:n.1411T>G
|
|
|
XR_001740209.2:n.1381T>G
|
|
|
XR_001740210.1:n.1241T>G
|
|
|
XR_002959553.1:n.1411T>G
|
|
|
XR_002959554.1:n.1411T>G
|
|
|
XR_241502.3:n.1381T>G
|
|
|
NM_020166.5:c.1288T>G
MANE Select
|
NP_064551.3:p.Tyr430Asp
|
|
NM_001293273.2:c.937T>G
|
NP_001280202.1:p.Tyr313Asp
|
|
NR_120639.2:n.1111T>G
|
|
|
NR_120640.2:n.1955T>G
|
|
|