ENST00000683611.1:n.1164C>G
|
|
|
ENST00000265104.5:c.13831C>G
MANE Select
|
ENSP00000265104.4:p.His4611Asp
|
|
ENST00000681290.1:c.13786C>G
|
ENSP00000505288.1:p.His4596Asp
|
|
ENST00000265104.4:c.13831C>G
|
ENSP00000265104.4:p.His4611Asp
|
|
NM_001369.2:c.13831C>G
|
NP_001360.1:p.His4611Asp
|
|
XM_005248262.2:c.13786C>G
|
XP_005248319.1:p.His4596Asp
|
|
XM_005248262.3:c.13939C>G
|
XP_005248319.2:p.His4647Asp
|
|
XM_017009177.1:c.13519C>G
|
XP_016864666.1:p.His4507Asp
|
|
XM_017009178.1:c.12844C>G
|
XP_016864667.1:p.His4282Asp
|
|
XM_017009179.2:c.12844C>G
|
XP_016864668.1:p.His4282Asp
|
|
XM_017009185.1:c.9028C>G
|
XP_016864674.1:p.His3010Asp
|
|
XM_017009186.1:c.8581C>G
|
XP_016864675.1:p.His2861Asp
|
|
XM_017009188.1:c.7918C>G
|
XP_016864677.1:p.His2640Asp
|
|
XM_024454388.1:c.12844C>G
|
XP_024310156.1:p.His4282Asp
|
|
XM_024454389.1:c.12433C>G
|
XP_024310157.1:p.His4145Asp
|
|
NM_001369.3:c.13831C>G
MANE Select
|
NP_001360.1:p.His4611Asp
|
|