ENST00000265104.5:c.11673C>G
MANE Select
|
ENSP00000265104.4:p.His3891Gln
|
|
ENST00000681290.1:c.11628C>G
|
ENSP00000505288.1:p.His3876Gln
|
|
ENST00000265104.4:c.11673C>G
|
ENSP00000265104.4:p.His3891Gln
|
|
NM_001369.2:c.11673C>G
|
NP_001360.1:p.His3891Gln
|
|
XM_005248262.2:c.11628C>G
|
XP_005248319.1:p.His3876Gln
|
|
XM_005248262.3:c.11781C>G
|
XP_005248319.2:p.His3927Gln
|
|
XM_017009177.1:c.11781C>G
|
XP_016864666.1:p.His3927Gln
|
|
XM_017009178.1:c.10686C>G
|
XP_016864667.1:p.His3562Gln
|
|
XM_017009179.2:c.10686C>G
|
XP_016864668.1:p.His3562Gln
|
|
XM_017009180.1:c.11781C>G
|
XP_016864669.1:p.His3927Gln
|
|
XM_017009181.1:c.11781C>G
|
XP_016864670.1:p.His3927Gln
|
|
XM_017009185.1:c.6870C>G
|
XP_016864674.1:p.His2290Gln
|
|
XM_017009186.1:c.6423C>G
|
XP_016864675.1:p.His2141Gln
|
|
XM_017009188.1:c.5760C>G
|
XP_016864677.1:p.His1920Gln
|
|
XM_024454388.1:c.10686C>G
|
XP_024310156.1:p.His3562Gln
|
|
XM_024454389.1:c.10275C>G
|
XP_024310157.1:p.His3425Gln
|
|
NM_001369.3:c.11673C>G
MANE Select
|
NP_001360.1:p.His3891Gln
|
|