ENST00000274008.5:c.2351G>A
MANE Select
|
ENSP00000274008.3:p.Arg784Gln
|
|
ENST00000675612.1:c.2420G>A
|
ENSP00000502453.1:p.Arg807Gln
|
|
ENST00000274008.4:c.2351G>A
|
ENSP00000274008.3:p.Arg784Gln
|
|
NM_145207.2:c.2351G>A
|
NP_660208.2:p.Arg784Gln
|
|
XM_005262783.3:c.2348G>A
|
XP_005262840.1:p.Arg783Gln
|
|
XM_011531678.1:c.2420G>A
|
XP_011529980.1:p.Arg807Gln
|
|
NM_001345856.1:c.2348G>A
|
NP_001332785.1:p.Arg783Gln
|
|
XM_011531678.2:c.2420G>A
|
XP_011529980.1:p.Arg807Gln
|
|
XM_017007825.1:c.2423G>A
|
XP_016863314.1:p.Arg808Gln
|
|
XM_017007826.1:c.2423G>A
|
XP_016863315.1:p.Arg808Gln
|
|
XM_017007828.1:c.2129G>A
|
XP_016863317.1:p.Arg710Gln
|
|
XM_017007829.1:c.1967G>A
|
XP_016863318.1:p.Arg656Gln
|
|
XR_001741151.1:n.2509G>A
|
|
|
NM_145207.3:c.2351G>A
MANE Select
|
NP_660208.2:p.Arg784Gln
|
|
NM_001345856.2:c.2348G>A
|
NP_001332785.1:p.Arg783Gln
|
|