ENST00000328300.11:c.3874A>C
MANE Select
|
ENSP00000331902.7:p.Asn1292His
|
|
ENST00000361603.7:c.3856A>C
|
ENSP00000354505.2:p.Asn1286His
|
|
ENST00000510690.2:n.368A>C
|
|
|
ENST00000328300.10:c.3874A>C
|
ENSP00000331902.6:p.Asn1292His
|
|
ENST00000361603.6:c.3856A>C
|
ENSP00000354505.2:p.Asn1286His
|
|
ENST00000489230.1:n.277A>C
|
|
|
ENST00000510690.1:n.368A>C
|
|
|
NM_000495.4:c.3856A>C
|
NP_000486.1:p.Asn1286His
|
|
NM_033380.2:c.3874A>C
|
NP_203699.1:p.Asn1292His
|
|
XM_005262070.2:c.3865A>C
|
XP_005262127.1:p.Asn1289His
|
|
XM_006724616.2:c.3874A>C
|
XP_006724679.1:p.Asn1292His
|
|
XM_011530849.1:c.3550A>C
|
XP_011529151.1:p.Asn1184His
|
|
XM_011530851.1:c.1447A>C
|
XP_011529153.1:p.Asn483His
|
|
XM_011530849.2:c.3889A>C
|
XP_011529151.2:p.Asn1297His
|
|
XM_017029259.2:c.3880A>C
|
XP_016884748.1:p.Asn1294His
|
|
XM_017029260.1:c.3871A>C
|
XP_016884749.1:p.Asn1291His
|
|
XM_017029261.1:c.3889A>C
|
XP_016884750.1:p.Asn1297His
|
|
XM_017029263.2:c.2209A>C
|
XP_016884752.1:p.Asn737His
|
|
NM_000495.5:c.3856A>C
|
NP_000486.1:p.Asn1286His
|
|
NM_033380.3:c.3874A>C
MANE Select
|
NP_203699.1:p.Asn1292His
|
|