ENST00000366159.9:n.1807T>A
|
|
|
ENST00000437813.8:c.*167T>A
|
ENSP00000513672.1:n.*167T>A
|
|
ENST00000440083.7:c.925T>A
|
ENSP00000413224.3:p.Tyr309Asn
|
|
ENST00000535038.2:n.888T>A
|
|
|
ENST00000535958.2:c.*533T>A
|
ENSP00000513673.1:n.*533T>A
|
|
ENST00000698337.1:n.696T>A
|
|
|
ENST00000698338.1:n.1120T>A
|
|
|
ENST00000698339.1:c.*201T>A
|
ENSP00000513670.1:n.*201T>A
|
|
ENST00000698340.1:c.632T>A
|
ENSP00000513671.1:p.Leu211Gln
|
|
ENST00000162749.7:c.706T>A
MANE Select
|
ENSP00000162749.2:p.Tyr236Asn
|
|
ENST00000162749.6:c.706T>A
|
ENSP00000162749.2:p.Tyr236Asn
|
|
ENST00000534885.5:c.*183T>A
|
ENSP00000441803.1:n.*183T>A
|
|
ENST00000535038.1:n.517T>A
|
|
|
ENST00000536717.5:n.610T>A
|
|
|
ENST00000537842.5:n.310T>A
|
|
|
ENST00000539372.5:c.706T>A
|
ENSP00000442059.1:p.Tyr236Asn
|
|
ENST00000540022.5:c.577T>A
|
ENSP00000438343.1:p.Tyr193Asn
|
|
ENST00000543359.5:n.118T>A
|
|
|
ENST00000543995.5:c.*293T>A
|
ENSP00000442405.1:n.*293T>A
|
|
NM_001065.3:c.706T>A , LRG_193t1:c.706T>A
|
NP_001056.1:p.Tyr236Asn
|
|
NM_001346091.1:c.382T>A
|
NP_001333020.1:p.Tyr128Asn
|
|
NM_001346092.1:c.247T>A
|
NP_001333021.1:p.Tyr83Asn
|
|
NR_144351.1:n.935T>A
|
|
|
NM_001065.4:c.706T>A
MANE Select
|
NP_001056.1:p.Tyr236Asn
|
|
NM_001346091.2:c.382T>A
|
NP_001333020.1:p.Tyr128Asn
|
|
NM_001346092.2:c.247T>A
|
NP_001333021.1:p.Tyr83Asn
|
|
NR_144351.2:n.894T>A
|
|
|