ENST00000439388.6:c.2260G=
MANE Select
|
ENSP00000403084.1:p.Ala754=
|
|
ENST00000371868.5:c.544G=
|
ENSP00000360934.1:p.Ala182=
|
|
ENST00000371872.8:c.2260G=
|
ENSP00000360938.4:p.Ala754=
|
|
ENST00000422262.6:c.1420G=
|
ENSP00000415537.3:p.Ala474=
|
|
ENST00000439388.5:c.2260G=
|
ENSP00000403084.1:p.Ala754=
|
|
NM_001134707.1:c.2260G=
|
NP_001128179.1:p.Ala754=
|
|
NM_007101.3:c.2260G=
|
NP_009032.2:p.Ala754=
|
|
XM_006716990.2:c.2260G=
|
XP_006717053.1:p.Ala754=
|
|
XM_011518333.1:c.2260G=
|
XP_011516635.1:p.Ala754=
|
|
XR_929726.1:n.2427G=
|
|
|
XR_929727.1:n.2427G=
|
|
|
XR_929728.1:n.2427G=
|
|
|
XM_017014367.1:c.2260G=
|
XP_016869856.1:p.Ala754=
|
|
XM_017014368.1:c.2260G=
|
XP_016869857.1:p.Ala754=
|
|
XR_001746213.1:n.2556G=
|
|
|
XR_001746214.1:n.3739G=
|
|
|
XR_001746215.1:n.2558G=
|
|
|
XR_001746216.1:n.2556G=
|
|
|
XR_001746217.1:n.2556G=
|
|
|
XR_001746218.1:n.2408G=
|
|
|
XR_002956762.1:n.2512G=
|
|
|
XR_929726.2:n.2427G=
|
|
|
NM_001134707.2:c.2260G=
MANE Select
|
NP_001128179.1:p.Ala754=
|
|
NM_007101.4:c.2260G=
|
NP_009032.2:p.Ala754=
|
|