ENST00000578493.2:n.721T>G
|
|
|
ENST00000699291.1:c.513T>G
|
ENSP00000514272.1:p.Pro171=
|
|
ENST00000699292.1:n.428T>G
|
|
|
ENST00000225275.4:c.1388T>G
MANE Select
|
ENSP00000225275.3:p.Leu463Arg
|
|
ENST00000225275.3:c.1388T>G
|
ENSP00000225275.3:p.Leu463Arg
|
|
NM_000250.1:c.1388T>G , LRG_84t1:c.1388T>G
|
NP_000241.1:p.Leu463Arg
|
|
XM_011524821.1:c.1574T>G
|
XP_011523123.1:p.Leu525Arg
|
|
XM_011524822.1:c.1103T>G
|
XP_011523124.1:p.Leu368Arg
|
|
XM_011524823.1:c.1413T>G
|
XP_011523125.1:p.Pro471=
|
|
NM_000250.2:c.1388T>G
MANE Select
|
NP_000241.1:p.Leu463Arg
|
|