ENST00000265104.5:c.11687C>A
MANE Select
|
ENSP00000265104.4:p.Thr3896Asn
|
|
ENST00000681290.1:c.11642C>A
|
ENSP00000505288.1:p.Thr3881Asn
|
|
ENST00000265104.4:c.11687C>A
|
ENSP00000265104.4:p.Thr3896Asn
|
|
NM_001369.2:c.11687C>A
|
NP_001360.1:p.Thr3896Asn
|
|
XM_005248262.2:c.11642C>A
|
XP_005248319.1:p.Thr3881Asn
|
|
XM_005248262.3:c.11795C>A
|
XP_005248319.2:p.Thr3932Asn
|
|
XM_017009177.1:c.11795C>A
|
XP_016864666.1:p.Thr3932Asn
|
|
XM_017009178.1:c.10700C>A
|
XP_016864667.1:p.Thr3567Asn
|
|
XM_017009179.2:c.10700C>A
|
XP_016864668.1:p.Thr3567Asn
|
|
XM_017009180.1:c.11795C>A
|
XP_016864669.1:p.Thr3932Asn
|
|
XM_017009181.1:c.11795C>A
|
XP_016864670.1:p.Thr3932Asn
|
|
XM_017009185.1:c.6884C>A
|
XP_016864674.1:p.Thr2295Asn
|
|
XM_017009186.1:c.6437C>A
|
XP_016864675.1:p.Thr2146Asn
|
|
XM_017009188.1:c.5774C>A
|
XP_016864677.1:p.Thr1925Asn
|
|
XM_024454388.1:c.10700C>A
|
XP_024310156.1:p.Thr3567Asn
|
|
XM_024454389.1:c.10289C>A
|
XP_024310157.1:p.Thr3430Asn
|
|
NM_001369.3:c.11687C>A
MANE Select
|
NP_001360.1:p.Thr3896Asn
|
|