ENST00000578493.2:n.766C>T
|
|
|
ENST00000699291.1:c.558C>T
|
ENSP00000514272.1:p.His186=
|
|
ENST00000699292.1:n.473C>T
|
|
|
ENST00000225275.4:c.1433C>T
MANE Select
|
ENSP00000225275.3:p.Thr478Met
|
|
ENST00000225275.3:c.1433C>T
|
ENSP00000225275.3:p.Thr478Met
|
|
NM_000250.1:c.1433C>T , LRG_84t1:c.1433C>T
|
NP_000241.1:p.Thr478Met
|
|
XM_011524821.1:c.1619C>T
|
XP_011523123.1:p.Thr540Met
|
|
XM_011524822.1:c.1148C>T
|
XP_011523124.1:p.Thr383Met
|
|
XM_011524823.1:c.1458C>T
|
XP_011523125.1:p.His486=
|
|
NM_000250.2:c.1433C>T
MANE Select
|
NP_000241.1:p.Thr478Met
|
|