ENST00000578493.2:n.757A>C
|
|
|
ENST00000699291.1:c.549A>C
|
ENSP00000514272.1:p.Val183=
|
|
ENST00000699292.1:n.464A>C
|
|
|
ENST00000225275.4:c.1424A>C
MANE Select
|
ENSP00000225275.3:p.Tyr475Ser
|
|
ENST00000225275.3:c.1424A>C
|
ENSP00000225275.3:p.Tyr475Ser
|
|
NM_000250.1:c.1424A>C , LRG_84t1:c.1424A>C
|
NP_000241.1:p.Tyr475Ser
|
|
XM_011524821.1:c.1610A>C
|
XP_011523123.1:p.Tyr537Ser
|
|
XM_011524822.1:c.1139A>C
|
XP_011523124.1:p.Tyr380Ser
|
|
XM_011524823.1:c.1449A>C
|
XP_011523125.1:p.Val483=
|
|
NM_000250.2:c.1424A>C
MANE Select
|
NP_000241.1:p.Tyr475Ser
|
|