ENST00000578493.2:n.712G>T
|
|
|
ENST00000699291.1:c.504G>T
|
ENSP00000514272.1:p.Pro168=
|
|
ENST00000699292.1:n.419G>T
|
|
|
ENST00000225275.4:c.1379G>T
MANE Select
|
ENSP00000225275.3:p.Arg460Leu
|
|
ENST00000225275.3:c.1379G>T
|
ENSP00000225275.3:p.Arg460Leu
|
|
NM_000250.1:c.1379G>T , LRG_84t1:c.1379G>T
|
NP_000241.1:p.Arg460Leu
|
|
XM_011524821.1:c.1565G>T
|
XP_011523123.1:p.Arg522Leu
|
|
XM_011524822.1:c.1094G>T
|
XP_011523124.1:p.Arg365Leu
|
|
XM_011524823.1:c.1404G>T
|
XP_011523125.1:p.Pro468=
|
|
NM_000250.2:c.1379G>T
MANE Select
|
NP_000241.1:p.Arg460Leu
|
|