ENST00000614565.5:c.1817T>A
MANE Select
|
ENSP00000484928.1:p.Ile606Asn
|
|
ENST00000543233.2:c.1595T>A
|
ENSP00000443301.1:p.Ile532Asn
|
|
ENST00000611855.4:c.1535T>A
|
ENSP00000480844.1:p.Ile512Asn
|
|
ENST00000614565.4:c.1817T>A
|
ENSP00000484928.1:p.Ile606Asn
|
|
NM_001252338.2:c.1706T>A
|
NP_001239267.1:p.Ile569Asn
|
|
NM_001252339.2:c.1595T>A
|
NP_001239268.1:p.Ile532Asn
|
|
NM_001794.4:c.1817T>A
|
NP_001785.2:p.Ile606Asn
|
|
NM_001794.5:c.1817T>A
MANE Select
|
NP_001785.2:p.Ile606Asn
|
|
NM_001252339.3:c.1595T>A
|
NP_001239268.1:p.Ile532Asn
|
|