ENST00000367698.4:c.1311C>T
MANE Select
|
ENSP00000356671.3:p.Asn437=
|
|
ENST00000367698.3:c.1311C>T
|
ENSP00000356671.3:p.Asn437=
|
|
ENST00000617423.4:c.696C>T
|
ENSP00000478688.1:p.Asn232=
|
|
NM_000488.3:c.1311C>T , LRG_577t1:c.1311C>T
|
NP_000479.1:p.Asn437=
|
|
XM_005245198.2:c.1167C>T
|
XP_005245255.1:p.Asn389=
|
|
NM_001365052.1:c.1167C>T
|
NP_001351981.1:p.Asn389=
|
|
NM_000488.4:c.1311C>T
MANE Select
|
NP_000479.1:p.Asn437=
|
|
NM_001365052.2:c.1167C>T
|
NP_001351981.1:p.Asn389=
|
|
NM_001386302.1:c.1434C>T
|
NP_001373231.1:p.Asn478=
|
|
NM_001386303.1:c.1392C>T
|
NP_001373232.1:p.Asn464=
|
|
NM_001386304.1:c.1290C>T
|
NP_001373233.1:p.Asn430=
|
|
NM_001386305.1:c.1254C>T
|
NP_001373234.1:p.Asn418=
|
|
NM_001386306.1:c.1095C>T
|
NP_001373235.1:p.Asn365=
|
|