|
NM_004239.4:c.4062A>C
MANE Select
|
NP_004230.2:p.Lys1354Asn
|
|
ENST00000267622.8:c.4062A>C
MANE Select
|
ENSP00000267622.4:p.Lys1354Asn
|
|
NM_001321851.1:c.4059A>C
|
NP_001308780.1:p.Lys1353Asn
|
|
NM_004239.3:c.4062A>C
|
NP_004230.2:p.Lys1354Asn
|
|
ENST00000554357.5:c.3208A>C
|
|
|
XM_005268214.2:c.2736A>C
|
XP_005268271.1:p.Lys912Asn
|
|
XM_005268215.2:c.1527+3726A>C
|
XP_005268272.1:n.1527+3726A>C
|
|
XM_006720321.2:c.4059A>C
|
XP_006720384.1:p.Lys1353Asn
|
|
XM_011537361.1:c.4062A>C
|
XP_011535663.1:p.Lys1354Asn
|
|
XM_017021787.2:c.3357A>C
|
XP_016877276.1:p.Lys1119Asn
|
|
XM_017021788.2:c.2736A>C
|
XP_016877277.1:p.Lys912Asn
|
|
XR_001750598.2:n.4511A>C
|
|
|
XR_943560.1:n.4517A>C
|
|
|
XR_943560.2:n.4511A>C
|
|