ENST00000366159.9:n.2119A=
|
|
|
ENST00000437813.8:c.*479A=
|
ENSP00000513672.1:n.*479A=
|
|
ENST00000440083.7:c.1237A=
|
ENSP00000413224.3:p.Lys413=
|
|
ENST00000535958.2:c.*845A=
|
ENSP00000513673.1:n.*845A=
|
|
ENST00000698337.1:n.979A=
|
|
|
ENST00000698338.1:n.1632A=
|
|
|
ENST00000698339.1:c.*513A=
|
ENSP00000513670.1:n.*513A=
|
|
ENST00000698340.1:c.*257A=
|
ENSP00000513671.1:n.*257A=
|
|
ENST00000162749.7:c.1018A=
MANE Select
|
ENSP00000162749.2:p.Lys340=
|
|
ENST00000162749.6:c.1018A=
|
ENSP00000162749.2:p.Lys340=
|
|
ENST00000534885.5:c.*495A=
|
ENSP00000441803.1:n.*495A=
|
|
ENST00000536717.5:n.922A=
|
|
|
ENST00000540022.5:c.889A=
|
ENSP00000438343.1:p.Lys297=
|
|
ENST00000543359.5:n.430A=
|
|
|
ENST00000543995.5:c.*605A=
|
ENSP00000442405.1:n.*605A=
|
|
NM_001065.3:c.1018A= , LRG_193t1:c.1018A=
|
NP_001056.1:p.Lys340=
|
|
NM_001346091.1:c.694A=
|
NP_001333020.1:p.Lys232=
|
|
NM_001346092.1:c.559A=
|
NP_001333021.1:p.Lys187=
|
|
NR_144351.1:n.1247A=
|
|
|
NM_001065.4:c.1018A=
MANE Select
|
NP_001056.1:p.Lys340=
|
|
NM_001346091.2:c.694A=
|
NP_001333020.1:p.Lys232=
|
|
NM_001346092.2:c.559A=
|
NP_001333021.1:p.Lys187=
|
|
NR_144351.2:n.1206A=
|
|
|