ENST00000578493.2:n.820A>T
|
|
|
ENST00000699291.1:c.612A>T
|
ENSP00000514272.1:n.612A>T
|
|
ENST00000699292.1:n.527A>T
|
|
|
ENST00000225275.4:c.1487A>T
MANE Select
|
ENSP00000225275.3:p.Asn496Ile
|
|
ENST00000225275.3:c.1487A>T
|
ENSP00000225275.3:p.Asn496Ile
|
|
NM_000250.1:c.1487A>T , LRG_84t1:c.1487A>T
|
NP_000241.1:p.Asn496Ile
|
|
XM_011524821.1:c.1673A>T
|
XP_011523123.1:p.Asn558Ile
|
|
XM_011524822.1:c.1202A>T
|
XP_011523124.1:p.Asn401Ile
|
|
XM_011524823.1:c.*36A>T
|
XP_011523125.1:n.*36A>T
|
|
NM_000250.2:c.1487A>T
MANE Select
|
NP_000241.1:p.Asn496Ile
|
|