ENST00000703162.1:n.148G>A
|
|
|
ENST00000281043.4:c.799G>A
MANE Select
|
ENSP00000281043.3:p.Asp267Asn
|
|
ENST00000638417.1:c.166G>A
|
ENSP00000491476.1:p.Asp56Asn
|
|
ENST00000281043.3:c.799G>A
|
ENSP00000281043.3:p.Asp267Asn
|
|
NM_001293228.1:c.799G>A
|
NP_001280157.1:p.Asp267Asn
|
|
NM_001293231.1:c.166G>A
|
NP_001280160.1:p.Asp56Asn
|
|
NM_001293233.1:c.*734G>A
|
NP_001280162.1:n.*734G>A
|
|
NM_005378.5:c.799G>A
|
NP_005369.2:p.Asp267Asn
|
|
NM_005378.6:c.799G>A
MANE Select
|
NP_005369.2:p.Asp267Asn
|
|
NM_001293228.2:c.799G>A
|
NP_001280157.1:p.Asp267Asn
|
|
NM_001293231.2:c.166G>A
|
NP_001280160.1:p.Asp56Asn
|
|
NM_001293233.2:c.*734G>A
|
NP_001280162.1:n.*734G>A
|
|