ENST00000682275.1:c.1149G=
|
ENSP00000507852.1:p.Trp383=
|
|
ENST00000683395.1:c.1090G=
|
|
|
ENST00000684087.1:c.1113G=
|
ENSP00000506978.1:p.Trp371=
|
|
ENST00000506362.2:c.864G=
|
ENSP00000424103.2:p.Trp288=
|
|
ENST00000673642.1:c.772G=
|
ENSP00000501242.1:p.Gly258=
|
|
ENST00000673991.1:c.1149G=
|
ENSP00000501033.1:p.Trp383=
|
|
ENST00000226760.5:c.1113G=
MANE Select
|
ENSP00000226760.1:p.Trp371=
|
|
ENST00000503569.5:c.1113G=
|
ENSP00000423337.1:p.Trp371=
|
|
ENST00000506362.1:c.746G=
|
|
|
ENST00000507765.1:n.1298G=
|
|
|
NM_001145853.1:c.1113G=
|
NP_001139325.1:p.Trp371=
|
|
NM_006005.3:c.1113G=
MANE Select
|
NP_005996.2:p.Trp371=
|
|
XM_017008586.1:c.1122G=
|
XP_016864075.1:p.Trp374=
|
|