ENST00000683611.1:n.1058T>G
|
|
|
ENST00000265104.5:c.13725T>G
MANE Select
|
ENSP00000265104.4:p.Thr4575=
|
|
ENST00000681290.1:c.13680T>G
|
ENSP00000505288.1:p.Thr4560=
|
|
ENST00000265104.4:c.13725T>G
|
ENSP00000265104.4:p.Thr4575=
|
|
NM_001369.2:c.13725T>G
|
NP_001360.1:p.Thr4575=
|
|
XM_005248262.2:c.13680T>G
|
XP_005248319.1:p.Thr4560=
|
|
XM_005248262.3:c.13833T>G
|
XP_005248319.2:p.Thr4611=
|
|
XM_017009177.1:c.13413T>G
|
XP_016864666.1:p.Thr4471=
|
|
XM_017009178.1:c.12738T>G
|
XP_016864667.1:p.Thr4246=
|
|
XM_017009179.2:c.12738T>G
|
XP_016864668.1:p.Thr4246=
|
|
XM_017009185.1:c.8922T>G
|
XP_016864674.1:p.Thr2974=
|
|
XM_017009186.1:c.8475T>G
|
XP_016864675.1:p.Thr2825=
|
|
XM_017009188.1:c.7812T>G
|
XP_016864677.1:p.Thr2604=
|
|
XM_024454388.1:c.12738T>G
|
XP_024310156.1:p.Thr4246=
|
|
XM_024454389.1:c.12327T>G
|
XP_024310157.1:p.Thr4109=
|
|
NM_001369.3:c.13725T>G
MANE Select
|
NP_001360.1:p.Thr4575=
|
|