ENST00000578493.2:n.761G>C
|
|
|
ENST00000699291.1:c.553G>C
|
ENSP00000514272.1:p.Ala185Pro
|
|
ENST00000699292.1:n.468G>C
|
|
|
ENST00000225275.4:c.1428G>C
MANE Select
|
ENSP00000225275.3:p.Leu476=
|
|
ENST00000225275.3:c.1428G>C
|
ENSP00000225275.3:p.Leu476=
|
|
NM_000250.1:c.1428G>C , LRG_84t1:c.1428G>C
|
NP_000241.1:p.Leu476=
|
|
XM_011524821.1:c.1614G>C
|
XP_011523123.1:p.Leu538=
|
|
XM_011524822.1:c.1143G>C
|
XP_011523124.1:p.Leu381=
|
|
XM_011524823.1:c.1453G>C
|
XP_011523125.1:p.Ala485Pro
|
|
NM_000250.2:c.1428G>C
MANE Select
|
NP_000241.1:p.Leu476=
|
|