ENST00000683611.1:n.1121C>T
|
|
|
ENST00000265104.5:c.13788C>T
MANE Select
|
ENSP00000265104.4:p.Asn4596=
|
|
ENST00000681290.1:c.13743C>T
|
ENSP00000505288.1:p.Asn4581=
|
|
ENST00000265104.4:c.13788C>T
|
ENSP00000265104.4:p.Asn4596=
|
|
NM_001369.2:c.13788C>T
|
NP_001360.1:p.Asn4596=
|
|
XM_005248262.2:c.13743C>T
|
XP_005248319.1:p.Asn4581=
|
|
XM_005248262.3:c.13896C>T
|
XP_005248319.2:p.Asn4632=
|
|
XM_017009177.1:c.13476C>T
|
XP_016864666.1:p.Asn4492=
|
|
XM_017009178.1:c.12801C>T
|
XP_016864667.1:p.Asn4267=
|
|
XM_017009179.2:c.12801C>T
|
XP_016864668.1:p.Asn4267=
|
|
XM_017009185.1:c.8985C>T
|
XP_016864674.1:p.Asn2995=
|
|
XM_017009186.1:c.8538C>T
|
XP_016864675.1:p.Asn2846=
|
|
XM_017009188.1:c.7875C>T
|
XP_016864677.1:p.Asn2625=
|
|
XM_024454388.1:c.12801C>T
|
XP_024310156.1:p.Asn4267=
|
|
XM_024454389.1:c.12390C>T
|
XP_024310157.1:p.Asn4130=
|
|
NM_001369.3:c.13788C>T
MANE Select
|
NP_001360.1:p.Asn4596=
|
|