ENST00000643759.2:c.7116C>T
MANE Select
|
ENSP00000495214.1:p.Thr2372=
|
|
ENST00000368147.8:c.7116C>T
|
ENSP00000357129.4:p.Thr2372=
|
|
ENST00000481212.5:n.557C>T
|
|
|
ENST00000498708.1:n.548C>T
|
|
|
ENST00000614909.4:c.7116C>T
|
ENSP00000482595.1:p.Thr2372=
|
|
NM_003126.2:c.7116C>T
|
NP_003117.2:p.Thr2372=
|
|
XM_011509916.1:c.7116C>T
|
XP_011508218.1:p.Thr2372=
|
|
XM_011509917.1:c.7098C>T
|
XP_011508219.1:p.Thr2366=
|
|
NM_003126.3:c.7116C>T
|
NP_003117.2:p.Thr2372=
|
|
XM_011509916.2:c.7116C>T
|
XP_011508218.1:p.Thr2372=
|
|
XM_011509917.3:c.7098C>T
|
XP_011508219.1:p.Thr2366=
|
|
NM_003126.4:c.7116C>T
MANE Select
|
NP_003117.2:p.Thr2372=
|
|