ENST00000225964.10:c.4180A>C
MANE Select
|
ENSP00000225964.6:p.Asn1394His
|
|
ENST00000225964.9:c.4180A>C
|
ENSP00000225964.5:p.Asn1394His
|
|
ENST00000510710.3:n.1145A>C
|
|
|
NM_000088.3:c.4180A>C , LRG_1t1:c.4180A>C
|
NP_000079.2:p.Asn1394His
|
|
XM_005257058.3:c.3910A>C
|
XP_005257115.2:p.Asn1304His
|
|
XM_005257059.3:c.3262A>C
|
XP_005257116.2:p.Asn1088His
|
|
XM_011524341.1:c.3982A>C
|
XP_011522643.1:p.Asn1328His
|
|
XM_005257058.4:c.3910A>C
|
XP_005257115.2:p.Asn1304His
|
|
XM_005257059.4:c.3262A>C
|
XP_005257116.2:p.Asn1088His
|
|
NM_000088.4:c.4180A>C
MANE Select
|
NP_000079.2:p.Asn1394His
|
|