ENST00000683611.1:n.1165A>G
|
|
|
ENST00000265104.5:c.13832A>G
MANE Select
|
ENSP00000265104.4:p.His4611Arg
|
|
ENST00000681290.1:c.13787A>G
|
ENSP00000505288.1:p.His4596Arg
|
|
ENST00000265104.4:c.13832A>G
|
ENSP00000265104.4:p.His4611Arg
|
|
NM_001369.2:c.13832A>G
|
NP_001360.1:p.His4611Arg
|
|
XM_005248262.2:c.13787A>G
|
XP_005248319.1:p.His4596Arg
|
|
XM_005248262.3:c.13940A>G
|
XP_005248319.2:p.His4647Arg
|
|
XM_017009177.1:c.13520A>G
|
XP_016864666.1:p.His4507Arg
|
|
XM_017009178.1:c.12845A>G
|
XP_016864667.1:p.His4282Arg
|
|
XM_017009179.2:c.12845A>G
|
XP_016864668.1:p.His4282Arg
|
|
XM_017009185.1:c.9029A>G
|
XP_016864674.1:p.His3010Arg
|
|
XM_017009186.1:c.8582A>G
|
XP_016864675.1:p.His2861Arg
|
|
XM_017009188.1:c.7919A>G
|
XP_016864677.1:p.His2640Arg
|
|
XM_024454388.1:c.12845A>G
|
XP_024310156.1:p.His4282Arg
|
|
XM_024454389.1:c.12434A>G
|
XP_024310157.1:p.His4145Arg
|
|
NM_001369.3:c.13832A>G
MANE Select
|
NP_001360.1:p.His4611Arg
|
|