ENST00000682028.1:c.1330T>A
|
ENSP00000507230.1:p.Tyr444Asn
|
|
ENST00000682268.1:n.1628T>A
|
|
|
ENST00000682676.1:n.731T>A
|
|
|
ENST00000682902.1:n.1632T>A
|
|
|
ENST00000683513.1:c.1330T>A
|
ENSP00000506809.1:p.Tyr444Asn
|
|
ENST00000263431.4:c.1330T>A
MANE Select
|
ENSP00000263431.3:p.Tyr444Asn
|
|
ENST00000263431.3:c.1330T>A
|
ENSP00000263431.3:p.Tyr444Asn
|
|
NM_001316329.1:c.1330T>A
|
NP_001303258.1:p.Tyr444Asn
|
|
NM_002739.3:c.1330T>A , LRG_669t1:c.1330T>A
|
NP_002730.1:p.Tyr444Asn
|
|
NM_002739.4:c.1330T>A
|
NP_002730.1:p.Tyr444Asn
|
|
XM_011527108.1:c.421T>A
|
XP_011525410.1:p.Tyr141Asn
|
|
NM_002739.5:c.1330T>A
MANE Select
|
NP_002730.1:p.Tyr444Asn
|
|
NM_001316329.2:c.1330T>A
|
NP_001303258.1:p.Tyr444Asn
|
|