ENST00000309383.6:c.2147C>A
MANE Select
|
ENSP00000310649.1:p.Thr716Asn
|
|
ENST00000309383.5:c.2147C>A
|
ENSP00000310649.1:p.Thr716Asn
|
|
ENST00000326848.7:c.1232C>A
|
ENSP00000320853.7:p.Thr411Asn
|
|
ENST00000590333.5:c.2195C>A
|
ENSP00000468190.1:p.Thr732Asn
|
|
NM_032430.1:c.2147C>A
|
NP_115806.1:p.Thr716Asn
|
|
XM_005259327.2:c.1877C>A
|
XP_005259384.1:p.Thr626Asn
|
|
XM_011527395.1:c.1904C>A
|
XP_011525697.1:p.Thr635Asn
|
|
XR_430213.2:n.2130C>A
|
|
|
XM_005259327.3:c.1877C>A
|
XP_005259384.1:p.Thr626Asn
|
|
XM_011527395.2:c.1619C>A
|
XP_011525697.2:p.Thr540Asn
|
|
XM_024451739.1:c.1922C>A
|
XP_024307507.1:p.Thr641Asn
|
|
XR_430213.4:n.2428C>A
|
|
|
NM_032430.2:c.2147C>A
MANE Select
|
NP_115806.1:p.Thr716Asn
|
|