ENST00000366159.9:n.2122T=
|
|
|
ENST00000437813.8:c.*482T=
|
ENSP00000513672.1:n.*482T=
|
|
ENST00000440083.7:c.1240T=
|
ENSP00000413224.3:p.Trp414=
|
|
ENST00000535958.2:c.*848T=
|
ENSP00000513673.1:n.*848T=
|
|
ENST00000698337.1:n.982T=
|
|
|
ENST00000698338.1:n.1635T=
|
|
|
ENST00000698339.1:c.*516T=
|
ENSP00000513670.1:n.*516T=
|
|
ENST00000698340.1:c.*260T=
|
ENSP00000513671.1:n.*260T=
|
|
ENST00000162749.7:c.1021T=
MANE Select
|
ENSP00000162749.2:p.Trp341=
|
|
ENST00000162749.6:c.1021T=
|
ENSP00000162749.2:p.Trp341=
|
|
ENST00000534885.5:c.*498T=
|
ENSP00000441803.1:n.*498T=
|
|
ENST00000536717.5:n.925T=
|
|
|
ENST00000540022.5:c.892T=
|
ENSP00000438343.1:p.Trp298=
|
|
ENST00000543359.5:n.433T=
|
|
|
ENST00000543995.5:c.*608T=
|
ENSP00000442405.1:n.*608T=
|
|
NM_001065.3:c.1021T= , LRG_193t1:c.1021T=
|
NP_001056.1:p.Trp341=
|
|
NM_001346091.1:c.697T=
|
NP_001333020.1:p.Trp233=
|
|
NM_001346092.1:c.562T=
|
NP_001333021.1:p.Trp188=
|
|
NR_144351.1:n.1250T=
|
|
|
NM_001065.4:c.1021T=
MANE Select
|
NP_001056.1:p.Trp341=
|
|
NM_001346091.2:c.697T=
|
NP_001333020.1:p.Trp233=
|
|
NM_001346092.2:c.562T=
|
NP_001333021.1:p.Trp188=
|
|
NR_144351.2:n.1209T=
|
|
|