ENST00000683611.1:n.1121C>A
|
|
|
ENST00000265104.5:c.13788C>A
MANE Select
|
ENSP00000265104.4:p.Asn4596Lys
|
|
ENST00000681290.1:c.13743C>A
|
ENSP00000505288.1:p.Asn4581Lys
|
|
ENST00000265104.4:c.13788C>A
|
ENSP00000265104.4:p.Asn4596Lys
|
|
NM_001369.2:c.13788C>A
|
NP_001360.1:p.Asn4596Lys
|
|
XM_005248262.2:c.13743C>A
|
XP_005248319.1:p.Asn4581Lys
|
|
XM_005248262.3:c.13896C>A
|
XP_005248319.2:p.Asn4632Lys
|
|
XM_017009177.1:c.13476C>A
|
XP_016864666.1:p.Asn4492Lys
|
|
XM_017009178.1:c.12801C>A
|
XP_016864667.1:p.Asn4267Lys
|
|
XM_017009179.2:c.12801C>A
|
XP_016864668.1:p.Asn4267Lys
|
|
XM_017009185.1:c.8985C>A
|
XP_016864674.1:p.Asn2995Lys
|
|
XM_017009186.1:c.8538C>A
|
XP_016864675.1:p.Asn2846Lys
|
|
XM_017009188.1:c.7875C>A
|
XP_016864677.1:p.Asn2625Lys
|
|
XM_024454388.1:c.12801C>A
|
XP_024310156.1:p.Asn4267Lys
|
|
XM_024454389.1:c.12390C>A
|
XP_024310157.1:p.Asn4130Lys
|
|
NM_001369.3:c.13788C>A
MANE Select
|
NP_001360.1:p.Asn4596Lys
|
|