ENST00000265104.5:c.9601A>T
MANE Select
|
ENSP00000265104.4:p.Asn3201Tyr
|
|
ENST00000681290.1:c.9556A>T
|
ENSP00000505288.1:p.Asn3186Tyr
|
|
ENST00000265104.4:c.9601A>T
|
ENSP00000265104.4:p.Asn3201Tyr
|
|
ENST00000504001.3:n.313A>T
|
|
|
NM_001369.2:c.9601A>T
|
NP_001360.1:p.Asn3201Tyr
|
|
XM_005248262.2:c.9556A>T
|
XP_005248319.1:p.Asn3186Tyr
|
|
XM_005248262.3:c.9709A>T
|
XP_005248319.2:p.Asn3237Tyr
|
|
XM_017009177.1:c.9709A>T
|
XP_016864666.1:p.Asn3237Tyr
|
|
XM_017009178.1:c.8614A>T
|
XP_016864667.1:p.Asn2872Tyr
|
|
XM_017009179.2:c.8614A>T
|
XP_016864668.1:p.Asn2872Tyr
|
|
XM_017009180.1:c.9709A>T
|
XP_016864669.1:p.Asn3237Tyr
|
|
XM_017009181.1:c.9709A>T
|
XP_016864670.1:p.Asn3237Tyr
|
|
XM_017009182.1:c.9709A>T
|
XP_016864671.1:p.Asn3237Tyr
|
|
XM_017009183.1:c.9709A>T
|
XP_016864672.1:p.Asn3237Tyr
|
|
XM_017009185.1:c.4798A>T
|
XP_016864674.1:p.Asn1600Tyr
|
|
XM_017009186.1:c.4351A>T
|
XP_016864675.1:p.Asn1451Tyr
|
|
XM_017009188.1:c.3688A>T
|
XP_016864677.1:p.Asn1230Tyr
|
|
XM_024454388.1:c.8614A>T
|
XP_024310156.1:p.Asn2872Tyr
|
|
XM_024454389.1:c.8203A>T
|
XP_024310157.1:p.Asn2735Tyr
|
|
NM_001369.3:c.9601A>T
MANE Select
|
NP_001360.1:p.Asn3201Tyr
|
|