ENST00000366159.9:n.1808A>T
|
|
|
ENST00000437813.8:c.*168A>T
|
ENSP00000513672.1:n.*168A>T
|
|
ENST00000440083.7:c.926A>T
|
ENSP00000413224.3:p.Tyr309Phe
|
|
ENST00000535038.2:n.889A>T
|
|
|
ENST00000535958.2:c.*534A>T
|
ENSP00000513673.1:n.*534A>T
|
|
ENST00000698337.1:n.697A>T
|
|
|
ENST00000698338.1:n.1121A>T
|
|
|
ENST00000698339.1:c.*202A>T
|
ENSP00000513670.1:n.*202A>T
|
|
ENST00000698340.1:c.633A>T
|
ENSP00000513671.1:p.Leu211=
|
|
ENST00000162749.7:c.707A>T
MANE Select
|
ENSP00000162749.2:p.Tyr236Phe
|
|
ENST00000162749.6:c.707A>T
|
ENSP00000162749.2:p.Tyr236Phe
|
|
ENST00000534885.5:c.*184A>T
|
ENSP00000441803.1:n.*184A>T
|
|
ENST00000535038.1:n.518A>T
|
|
|
ENST00000536717.5:n.611A>T
|
|
|
ENST00000537842.5:n.311A>T
|
|
|
ENST00000539372.5:c.707A>T
|
ENSP00000442059.1:p.Tyr236Phe
|
|
ENST00000540022.5:c.578A>T
|
ENSP00000438343.1:p.Tyr193Phe
|
|
ENST00000543359.5:n.119A>T
|
|
|
ENST00000543995.5:c.*294A>T
|
ENSP00000442405.1:n.*294A>T
|
|
NM_001065.3:c.707A>T , LRG_193t1:c.707A>T
|
NP_001056.1:p.Tyr236Phe
|
|
NM_001346091.1:c.383A>T
|
NP_001333020.1:p.Tyr128Phe
|
|
NM_001346092.1:c.248A>T
|
NP_001333021.1:p.Tyr83Phe
|
|
NR_144351.1:n.936A>T
|
|
|
NM_001065.4:c.707A>T
MANE Select
|
NP_001056.1:p.Tyr236Phe
|
|
NM_001346091.2:c.383A>T
|
NP_001333020.1:p.Tyr128Phe
|
|
NM_001346092.2:c.248A>T
|
NP_001333021.1:p.Tyr83Phe
|
|
NR_144351.2:n.895A>T
|
|
|