ENST00000225964.10:c.4336G>A
MANE Select
|
ENSP00000225964.6:p.Asp1446Asn
|
|
ENST00000225964.9:c.4336G>A
|
ENSP00000225964.5:p.Asp1446Asn
|
|
NM_000088.3:c.4336G>A , LRG_1t1:c.4336G>A
|
NP_000079.2:p.Asp1446Asn
|
|
XM_005257058.3:c.4066G>A
|
XP_005257115.2:p.Asp1356Asn
|
|
XM_005257059.3:c.3418G>A
|
XP_005257116.2:p.Asp1140Asn
|
|
XM_011524341.1:c.4138G>A
|
XP_011522643.1:p.Asp1380Asn
|
|
XM_005257058.4:c.4066G>A
|
XP_005257115.2:p.Asp1356Asn
|
|
XM_005257059.4:c.3418G>A
|
XP_005257116.2:p.Asp1140Asn
|
|
NM_000088.4:c.4336G>A
MANE Select
|
NP_000079.2:p.Asp1446Asn
|
|