ENST00000265104.5:c.12628T>A
MANE Select
|
ENSP00000265104.4:p.Tyr4210Asn
|
|
ENST00000681290.1:c.12583T>A
|
ENSP00000505288.1:p.Tyr4195Asn
|
|
ENST00000265104.4:c.12628T>A
|
ENSP00000265104.4:p.Tyr4210Asn
|
|
NM_001369.2:c.12628T>A
|
NP_001360.1:p.Tyr4210Asn
|
|
XM_005248262.2:c.12583T>A
|
XP_005248319.1:p.Tyr4195Asn
|
|
XM_005248262.3:c.12736T>A
|
XP_005248319.2:p.Tyr4246Asn
|
|
XM_017009177.1:c.12736T>A
|
XP_016864666.1:p.Tyr4246Asn
|
|
XM_017009178.1:c.11641T>A
|
XP_016864667.1:p.Tyr3881Asn
|
|
XM_017009179.2:c.11641T>A
|
XP_016864668.1:p.Tyr3881Asn
|
|
XM_017009180.1:c.12736T>A
|
XP_016864669.1:p.Tyr4246Asn
|
|
XM_017009185.1:c.7825T>A
|
XP_016864674.1:p.Tyr2609Asn
|
|
XM_017009186.1:c.7378T>A
|
XP_016864675.1:p.Tyr2460Asn
|
|
XM_017009188.1:c.6715T>A
|
XP_016864677.1:p.Tyr2239Asn
|
|
XM_024454388.1:c.11641T>A
|
XP_024310156.1:p.Tyr3881Asn
|
|
XM_024454389.1:c.11230T>A
|
XP_024310157.1:p.Tyr3744Asn
|
|
NM_001369.3:c.12628T>A
MANE Select
|
NP_001360.1:p.Tyr4210Asn
|
|