ENST00000263967.4:c.2762T>A
MANE Select
|
ENSP00000263967.3:p.Ile921Asn
|
|
ENST00000462255.2:n.1785T>A
|
|
|
ENST00000643187.1:c.2762T>A
|
ENSP00000493507.1:p.Ile921Asn
|
|
ENST00000674534.1:n.3670T>A
|
|
|
ENST00000674622.1:c.1183T>A
|
ENSP00000502417.1:n.1183T>A
|
|
ENST00000675467.1:n.5569T>A
|
|
|
ENST00000675786.1:c.*1329T>A
|
ENSP00000502323.1:n.*1329T>A
|
|
ENST00000675796.1:n.2657T>A
|
|
|
ENST00000263967.3:c.2762T>A
|
ENSP00000263967.3:p.Ile921Asn
|
|
NM_006218.2:c.2762T>A , LRG_310t1:c.2762T>A
|
NP_006209.2:p.Ile921Asn
|
|
XM_006713658.2:c.2762T>A
|
XP_006713721.1:p.Ile921Asn
|
|
XM_011512894.1:c.2762T>A
|
XP_011511196.1:p.Ile921Asn
|
|
NM_006218.3:c.2762T>A
|
NP_006209.2:p.Ile921Asn
|
|
XM_006713658.4:c.2762T>A
|
XP_006713721.1:p.Ile921Asn
|
|
XM_011512894.2:c.2762T>A
|
XP_011511196.1:p.Ile921Asn
|
|
NM_006218.4:c.2762T>A
MANE Select
|
NP_006209.2:p.Ile921Asn
|
|