ENST00000225964.10:c.4207A>G
MANE Select
|
ENSP00000225964.6:p.Asn1403Asp
|
|
ENST00000225964.9:c.4207A>G
|
ENSP00000225964.5:p.Asn1403Asp
|
|
NM_000088.3:c.4207A>G , LRG_1t1:c.4207A>G
|
NP_000079.2:p.Asn1403Asp
|
|
XM_005257058.3:c.3937A>G
|
XP_005257115.2:p.Asn1313Asp
|
|
XM_005257059.3:c.3289A>G
|
XP_005257116.2:p.Asn1097Asp
|
|
XM_011524341.1:c.4009A>G
|
XP_011522643.1:p.Asn1337Asp
|
|
XM_005257058.4:c.3937A>G
|
XP_005257115.2:p.Asn1313Asp
|
|
XM_005257059.4:c.3289A>G
|
XP_005257116.2:p.Asn1097Asp
|
|
NM_000088.4:c.4207A>G
MANE Select
|
NP_000079.2:p.Asn1403Asp
|
|