ENST00000265104.5:c.8140A>C
MANE Select
|
ENSP00000265104.4:p.Asn2714His
|
|
ENST00000681290.1:c.8095A>C
|
ENSP00000505288.1:p.Asn2699His
|
|
ENST00000265104.4:c.8140A>C
|
ENSP00000265104.4:p.Asn2714His
|
|
NM_001369.2:c.8140A>C
|
NP_001360.1:p.Asn2714His
|
|
XM_005248262.2:c.8095A>C
|
XP_005248319.1:p.Asn2699His
|
|
XM_011513990.1:c.8140A>C
|
XP_011512292.1:p.Asn2714His
|
|
XR_925598.1:n.8347A>C
|
|
|
XM_005248262.3:c.8248A>C
|
XP_005248319.2:p.Asn2750His
|
|
XM_017009177.1:c.8248A>C
|
XP_016864666.1:p.Asn2750His
|
|
XM_017009178.1:c.7153A>C
|
XP_016864667.1:p.Asn2385His
|
|
XM_017009179.2:c.7153A>C
|
XP_016864668.1:p.Asn2385His
|
|
XM_017009180.1:c.8248A>C
|
XP_016864669.1:p.Asn2750His
|
|
XM_017009181.1:c.8248A>C
|
XP_016864670.1:p.Asn2750His
|
|
XM_017009182.1:c.8248A>C
|
XP_016864671.1:p.Asn2750His
|
|
XM_017009183.1:c.8248A>C
|
XP_016864672.1:p.Asn2750His
|
|
XM_017009184.1:c.8248A>C
|
XP_016864673.1:p.Asn2750His
|
|
XM_017009185.1:c.3337A>C
|
XP_016864674.1:p.Asn1113His
|
|
XM_017009186.1:c.2890A>C
|
XP_016864675.1:p.Asn964His
|
|
XM_017009188.1:c.2227A>C
|
XP_016864677.1:p.Asn743His
|
|
XM_024454388.1:c.7153A>C
|
XP_024310156.1:p.Asn2385His
|
|
XM_024454389.1:c.6742A>C
|
XP_024310157.1:p.Asn2248His
|
|
XR_001742034.1:n.8265A>C
|
|
|
XR_001742035.1:n.8265A>C
|
|
|
NM_001369.3:c.8140A>C
MANE Select
|
NP_001360.1:p.Asn2714His
|
|