ENST00000367698.4:c.1250G>A
MANE Select
|
ENSP00000356671.3:p.Ser417Asn
|
|
ENST00000367698.3:c.1250G>A
|
ENSP00000356671.3:p.Ser417Asn
|
|
ENST00000617423.4:c.635G>A
|
ENSP00000478688.1:p.Ser212Asn
|
|
NM_000488.3:c.1250G>A , LRG_577t1:c.1250G>A
|
NP_000479.1:p.Ser417Asn
|
|
XM_005245198.2:c.1106G>A
|
XP_005245255.1:p.Ser369Asn
|
|
NM_001365052.1:c.1106G>A
|
NP_001351981.1:p.Ser369Asn
|
|
NM_000488.4:c.1250G>A
MANE Select
|
NP_000479.1:p.Ser417Asn
|
|
NM_001365052.2:c.1106G>A
|
NP_001351981.1:p.Ser369Asn
|
|
NM_001386302.1:c.1373G>A
|
NP_001373231.1:p.Ser458Asn
|
|
NM_001386303.1:c.1331G>A
|
NP_001373232.1:p.Ser444Asn
|
|
NM_001386304.1:c.1229G>A
|
NP_001373233.1:p.Ser410Asn
|
|
NM_001386305.1:c.1193G>A
|
NP_001373234.1:p.Ser398Asn
|
|
NM_001386306.1:c.1034G>A
|
NP_001373235.1:p.Ser345Asn
|
|