ENST00000265104.5:c.10904A>T
MANE Select
|
ENSP00000265104.4:p.Asn3635Ile
|
|
ENST00000681290.1:c.10859A>T
|
ENSP00000505288.1:p.Asn3620Ile
|
|
ENST00000265104.4:c.10904A>T
|
ENSP00000265104.4:p.Asn3635Ile
|
|
NM_001369.2:c.10904A>T
|
NP_001360.1:p.Asn3635Ile
|
|
XM_005248262.2:c.10859A>T
|
XP_005248319.1:p.Asn3620Ile
|
|
XM_005248262.3:c.11012A>T
|
XP_005248319.2:p.Asn3671Ile
|
|
XM_017009177.1:c.11012A>T
|
XP_016864666.1:p.Asn3671Ile
|
|
XM_017009178.1:c.9917A>T
|
XP_016864667.1:p.Asn3306Ile
|
|
XM_017009179.2:c.9917A>T
|
XP_016864668.1:p.Asn3306Ile
|
|
XM_017009180.1:c.11012A>T
|
XP_016864669.1:p.Asn3671Ile
|
|
XM_017009181.1:c.11012A>T
|
XP_016864670.1:p.Asn3671Ile
|
|
XM_017009182.1:c.11012A>T
|
XP_016864671.1:p.Asn3671Ile
|
|
XM_017009185.1:c.6101A>T
|
XP_016864674.1:p.Asn2034Ile
|
|
XM_017009186.1:c.5654A>T
|
XP_016864675.1:p.Asn1885Ile
|
|
XM_017009188.1:c.4991A>T
|
XP_016864677.1:p.Asn1664Ile
|
|
XM_024454388.1:c.9917A>T
|
XP_024310156.1:p.Asn3306Ile
|
|
XM_024454389.1:c.9506A>T
|
XP_024310157.1:p.Asn3169Ile
|
|
NM_001369.3:c.10904A>T
MANE Select
|
NP_001360.1:p.Asn3635Ile
|
|