ENST00000218099.7:c.592G>A
MANE Select
|
ENSP00000218099.2:p.Asp198Asn
|
|
ENST00000643157.1:n.1259G>A
|
|
|
ENST00000218099.6:c.592G>A
|
ENSP00000218099.2:p.Asp198Asn
|
|
ENST00000394090.2:c.478G>A
|
ENSP00000377650.2:p.Asp160Asn
|
|
NM_000133.3:c.592G>A , LRG_556t1:c.592G>A
|
NP_000124.1:p.Asp198Asn
|
|
NM_001313913.1:c.478G>A
|
NP_001300842.1:p.Asp160Asn
|
|
XM_005262397.3:c.463G>A
|
XP_005262454.1:p.Asp155Asn
|
|
XM_005262397.4:c.463G>A
|
XP_005262454.1:p.Asp155Asn
|
|
NM_000133.4:c.592G>A
MANE Select
|
NP_000124.1:p.Asp198Asn
|
|
NM_001313913.2:c.478G>A
|
NP_001300842.1:p.Asp160Asn
|
|