ENST00000683611.1:n.1197G>A
|
|
|
ENST00000265104.5:c.13864G>A
MANE Select
|
ENSP00000265104.4:p.Asp4622Asn
|
|
ENST00000681290.1:c.13819G>A
|
ENSP00000505288.1:p.Asp4607Asn
|
|
ENST00000265104.4:c.13864G>A
|
ENSP00000265104.4:p.Asp4622Asn
|
|
NM_001369.2:c.13864G>A
|
NP_001360.1:p.Asp4622Asn
|
|
XM_005248262.2:c.13819G>A
|
XP_005248319.1:p.Asp4607Asn
|
|
XM_005248262.3:c.13972G>A
|
XP_005248319.2:p.Asp4658Asn
|
|
XM_017009177.1:c.13552G>A
|
XP_016864666.1:p.Asp4518Asn
|
|
XM_017009178.1:c.12877G>A
|
XP_016864667.1:p.Asp4293Asn
|
|
XM_017009179.2:c.12877G>A
|
XP_016864668.1:p.Asp4293Asn
|
|
XM_017009185.1:c.9061G>A
|
XP_016864674.1:p.Asp3021Asn
|
|
XM_017009186.1:c.8614G>A
|
XP_016864675.1:p.Asp2872Asn
|
|
XM_017009188.1:c.7951G>A
|
XP_016864677.1:p.Asp2651Asn
|
|
XM_024454388.1:c.12877G>A
|
XP_024310156.1:p.Asp4293Asn
|
|
XM_024454389.1:c.12466G>A
|
XP_024310157.1:p.Asp4156Asn
|
|
NM_001369.3:c.13864G>A
MANE Select
|
NP_001360.1:p.Asp4622Asn
|
|