ENST00000265104.5:c.11001C>G
MANE Select
|
ENSP00000265104.4:p.Asn3667Lys
|
|
ENST00000681290.1:c.10956C>G
|
ENSP00000505288.1:p.Asn3652Lys
|
|
ENST00000265104.4:c.11001C>G
|
ENSP00000265104.4:p.Asn3667Lys
|
|
NM_001369.2:c.11001C>G
|
NP_001360.1:p.Asn3667Lys
|
|
XM_005248262.2:c.10956C>G
|
XP_005248319.1:p.Asn3652Lys
|
|
XM_005248262.3:c.11109C>G
|
XP_005248319.2:p.Asn3703Lys
|
|
XM_017009177.1:c.11109C>G
|
XP_016864666.1:p.Asn3703Lys
|
|
XM_017009178.1:c.10014C>G
|
XP_016864667.1:p.Asn3338Lys
|
|
XM_017009179.2:c.10014C>G
|
XP_016864668.1:p.Asn3338Lys
|
|
XM_017009180.1:c.11109C>G
|
XP_016864669.1:p.Asn3703Lys
|
|
XM_017009181.1:c.11109C>G
|
XP_016864670.1:p.Asn3703Lys
|
|
XM_017009182.1:c.11109C>G
|
XP_016864671.1:p.Asn3703Lys
|
|
XM_017009185.1:c.6198C>G
|
XP_016864674.1:p.Asn2066Lys
|
|
XM_017009186.1:c.5751C>G
|
XP_016864675.1:p.Asn1917Lys
|
|
XM_017009188.1:c.5088C>G
|
XP_016864677.1:p.Asn1696Lys
|
|
XM_024454388.1:c.10014C>G
|
XP_024310156.1:p.Asn3338Lys
|
|
XM_024454389.1:c.9603C>G
|
XP_024310157.1:p.Asn3201Lys
|
|
NM_001369.3:c.11001C>G
MANE Select
|
NP_001360.1:p.Asn3667Lys
|
|