ENST00000578493.2:n.738C>T
|
|
|
ENST00000699291.1:c.530C>T
|
ENSP00000514272.1:p.Ala177Val
|
|
ENST00000699292.1:n.445C>T
|
|
|
ENST00000225275.4:c.1405C>T
MANE Select
|
ENSP00000225275.3:p.Pro469Ser
|
|
ENST00000225275.3:c.1405C>T
|
ENSP00000225275.3:p.Pro469Ser
|
|
NM_000250.1:c.1405C>T , LRG_84t1:c.1405C>T
|
NP_000241.1:p.Pro469Ser
|
|
XM_011524821.1:c.1591C>T
|
XP_011523123.1:p.Pro531Ser
|
|
XM_011524822.1:c.1120C>T
|
XP_011523124.1:p.Pro374Ser
|
|
XM_011524823.1:c.1430C>T
|
XP_011523125.1:p.Ala477Val
|
|
NM_000250.2:c.1405C>T
MANE Select
|
NP_000241.1:p.Pro469Ser
|
|