ENST00000578493.2:n.706C>G
|
|
|
ENST00000699291.1:c.498C>G
|
ENSP00000514272.1:p.His166Gln
|
|
ENST00000699292.1:n.413C>G
|
|
|
ENST00000225275.4:c.1373C>G
MANE Select
|
ENSP00000225275.3:p.Thr458Ser
|
|
ENST00000225275.3:c.1373C>G
|
ENSP00000225275.3:p.Thr458Ser
|
|
NM_000250.1:c.1373C>G , LRG_84t1:c.1373C>G
|
NP_000241.1:p.Thr458Ser
|
|
XM_011524821.1:c.1559C>G
|
XP_011523123.1:p.Thr520Ser
|
|
XM_011524822.1:c.1088C>G
|
XP_011523124.1:p.Thr363Ser
|
|
XM_011524823.1:c.1398C>G
|
XP_011523125.1:p.His466Gln
|
|
NM_000250.2:c.1373C>G
MANE Select
|
NP_000241.1:p.Thr458Ser
|
|