ENST00000254108.12:c.538G>A
MANE Select
|
ENSP00000254108.8:p.Asp180Asn
|
|
ENST00000254108.11:c.538G>A
|
ENSP00000254108.7:p.Asp180Asn
|
|
ENST00000380244.7:c.535G>A
|
ENSP00000369594.3:p.Asp179Asn
|
|
ENST00000487509.6:n.603G>A
|
|
|
ENST00000566605.5:c.538G>A
|
ENSP00000455073.1:p.Asp180Asn
|
|
ENST00000568685.1:c.538G>A
|
ENSP00000455282.1:p.Asp180Asn
|
|
NM_001170634.1:c.535G>A
|
NP_001164105.1:p.Asp179Asn
|
|
NM_001170937.1:c.526G>A
|
NP_001164408.1:p.Asp176Asn
|
|
NM_004960.3:c.538G>A , LRG_655t1:c.538G>A
|
NP_004951.1:p.Asp180Asn
|
|
NR_028388.2:n.643G>A
|
|
|
XM_005255233.3:c.-43G>A
|
XP_005255290.1:n.-43G>A
|
|
XM_011545781.1:c.532G>A
|
XP_011544083.1:p.Asp178Asn
|
|
XM_011545782.1:c.-43G>A
|
XP_011544084.1:n.-43G>A
|
|
XM_005255233.5:c.-43G>A
|
XP_005255290.1:n.-43G>A
|
|
XM_011545782.2:c.-43G>A
|
XP_011544084.1:n.-43G>A
|
|
XM_024450221.1:c.529G>A
|
XP_024305989.1:p.Asp177Asn
|
|
NM_004960.4:c.538G>A
MANE Select
|
NP_004951.1:p.Asp180Asn
|
|