ENST00000683611.1:n.1090T>A
|
|
|
ENST00000265104.5:c.13757T>A
MANE Select
|
ENSP00000265104.4:p.Ile4586Asn
|
|
ENST00000681290.1:c.13712T>A
|
ENSP00000505288.1:p.Ile4571Asn
|
|
ENST00000265104.4:c.13757T>A
|
ENSP00000265104.4:p.Ile4586Asn
|
|
NM_001369.2:c.13757T>A
|
NP_001360.1:p.Ile4586Asn
|
|
XM_005248262.2:c.13712T>A
|
XP_005248319.1:p.Ile4571Asn
|
|
XM_005248262.3:c.13865T>A
|
XP_005248319.2:p.Ile4622Asn
|
|
XM_017009177.1:c.13445T>A
|
XP_016864666.1:p.Ile4482Asn
|
|
XM_017009178.1:c.12770T>A
|
XP_016864667.1:p.Ile4257Asn
|
|
XM_017009179.2:c.12770T>A
|
XP_016864668.1:p.Ile4257Asn
|
|
XM_017009185.1:c.8954T>A
|
XP_016864674.1:p.Ile2985Asn
|
|
XM_017009186.1:c.8507T>A
|
XP_016864675.1:p.Ile2836Asn
|
|
XM_017009188.1:c.7844T>A
|
XP_016864677.1:p.Ile2615Asn
|
|
XM_024454388.1:c.12770T>A
|
XP_024310156.1:p.Ile4257Asn
|
|
XM_024454389.1:c.12359T>A
|
XP_024310157.1:p.Ile4120Asn
|
|
NM_001369.3:c.13757T>A
MANE Select
|
NP_001360.1:p.Ile4586Asn
|
|