ENST00000578493.2:n.805C>T
|
|
|
ENST00000699291.1:c.597C>T
|
ENSP00000514272.1:n.597C>T
|
|
ENST00000699292.1:n.512C>T
|
|
|
ENST00000225275.4:c.1472C>T
MANE Select
|
ENSP00000225275.3:p.Ala491Val
|
|
ENST00000225275.3:c.1472C>T
|
ENSP00000225275.3:p.Ala491Val
|
|
NM_000250.1:c.1472C>T , LRG_84t1:c.1472C>T
|
NP_000241.1:p.Ala491Val
|
|
XM_011524821.1:c.1658C>T
|
XP_011523123.1:p.Ala553Val
|
|
XM_011524822.1:c.1187C>T
|
XP_011523124.1:p.Ala396Val
|
|
XM_011524823.1:c.*21C>T
|
XP_011523125.1:n.*21C>T
|
|
NM_000250.2:c.1472C>T
MANE Select
|
NP_000241.1:p.Ala491Val
|
|