|
NM_020166.5:c.288T>G
MANE Select
|
NP_064551.3:p.Tyr96Ter
|
|
ENST00000265594.9:c.288T>G
MANE Select
|
ENSP00000265594.4:p.Tyr96Ter
|
|
NM_001293273.1:c.59T>G
|
NP_001280202.1:p.Ile20Ser
|
|
NM_001293273.2:c.59T>G
|
NP_001280202.1:p.Ile20Ser
|
|
NM_001363880.1:c.-40T>G
|
NP_001350809.1:n.-40T>G
|
|
NM_020166.4:c.288T>G
|
NP_064551.3:p.Tyr96Ter
|
|
NR_120639.1:n.283+7785T>G
|
|
|
NR_120639.2:n.192+7785T>G
|
|
|
NR_120640.1:n.955T>G
|
|
|
NR_120640.2:n.955T>G
|
|
|
ENST00000265594.8:c.288T>G
|
ENSP00000265594.4:p.Tyr96Ter
|
|
ENST00000466650.5:c.*7T>G
|
ENSP00000418979.1:n.*7T>G
|
|
ENST00000476176.5:c.147T>G
|
ENSP00000420433.1:p.Tyr49Ter
|
|
ENST00000486226.1:c.*45T>G
|
ENSP00000420223.1:n.*45T>G
|
|
ENST00000487634.5:c.136+7785T>G
|
ENSP00000420591.1:n.136+7785T>G
|
|
ENST00000490284.5:c.89+12578T>G
|
ENSP00000419328.1:n.89+12578T>G
|
|
ENST00000492597.5:c.-40T>G
|
ENSP00000419898.1:n.-40T>G
|
|
ENST00000495767.5:c.136+7785T>G
|
ENSP00000419658.1:n.136+7785T>G
|
|
ENST00000497830.5:c.*7T>G
|
ENSP00000420088.1:n.*7T>G
|
|
ENST00000497959.5:c.174T>G
|
ENSP00000420648.1:p.Tyr58Ter
|
|
ENST00000539926.5:c.-40T>G
|
ENSP00000441253.2:n.-40T>G
|
|
ENST00000610757.4:c.-40T>G
|
ENSP00000480435.1:n.-40T>G
|
|
ENST00000629669.2:c.174T>G
|
ENSP00000486824.1:p.Tyr58Ter
|
|
XM_006713702.1:c.-40T>G
|
XP_006713765.1:n.-40T>G
|
|
XM_011512992.1:c.174T>G
|
XP_011511294.1:p.Tyr58Ter
|
|
XM_011512992.2:c.174T>G
|
XP_011511294.1:p.Tyr58Ter
|
|
XM_011512993.1:c.288T>G
|
XP_011511295.1:p.Tyr96Ter
|
|
XR_001740207.2:n.411T>G
|
|
|
XR_001740208.2:n.411T>G
|
|
|
XR_001740209.2:n.381T>G
|
|
|
XR_001740210.1:n.241T>G
|
|
|
XR_002959553.1:n.411T>G
|
|
|
XR_002959554.1:n.411T>G
|
|
|
XR_241502.2:n.435T>G
|
|
|
XR_241502.3:n.381T>G
|
|
|
XR_924159.1:n.435T>G
|
|
