ENST00000262493.12:c.995T>A
MANE Select
|
ENSP00000262493.6:p.Ile332Asn
|
|
ENST00000562316.6:c.545-1120T>A
|
ENSP00000457238.2:n.545-1120T>A
|
|
ENST00000564727.2:c.299T>A
|
ENSP00000454971.2:p.Ile100Asn
|
|
ENST00000568375.2:c.233T>A
|
|
|
ENST00000638210.1:n.1295T>A
|
|
|
ENST00000638705.1:c.995T>A
|
ENSP00000491223.1:p.Ile332Asn
|
|
ENST00000638836.1:n.905T>A
|
|
|
ENST00000639251.1:n.896T>A
|
|
|
ENST00000639268.1:c.630T>A
|
|
|
ENST00000639341.1:c.520T>A
|
|
|
ENST00000639770.1:c.1033T>A
|
ENSP00000491999.1:n.1033T>A
|
|
ENST00000640390.1:n.925T>A
|
|
|
ENST00000640469.1:c.359T>A
|
ENSP00000491875.1:p.Ile120Asn
|
|
ENST00000640560.1:n.771T>A
|
|
|
ENST00000640893.1:c.*393T>A
|
ENSP00000492677.1:n.*393T>A
|
|
ENST00000262493.10:c.995T>A
|
ENSP00000262493.6:p.Ile332Asn
|
|
ENST00000564727.1:c.215T>A
|
ENSP00000454971.1:p.Ile72Asn
|
|
ENST00000568375.1:n.233T>A
|
|
|
NM_020988.2:c.995T>A
|
NP_066268.1:p.Ile332Asn
|
|
XM_011523003.1:c.869T>A
|
XP_011521305.1:p.Ile290Asn
|
|
XM_011523003.3:c.869T>A
|
XP_011521305.1:p.Ile290Asn
|
|
NM_020988.3:c.995T>A
MANE Select
|
NP_066268.1:p.Ile332Asn
|
|