ENST00000399820.8:c.2457G>C
MANE Select
|
ENSP00000382717.3:p.Gln819His
|
|
ENST00000399820.7:c.2457G>C
|
ENSP00000382717.3:p.Gln819His
|
|
ENST00000506869.5:c.*2038G>C
|
ENSP00000424319.1:n.*2038G>C
|
|
ENST00000512095.5:n.1455G>C
|
|
|
NM_025132.3:c.2457G>C
|
NP_079408.3:p.Gln819His
|
|
XM_011513724.1:c.2469G>C
|
XP_011512026.1:p.Gln823His
|
|
XM_011513725.1:c.2403G>C
|
XP_011512027.1:p.Gln801His
|
|
XM_011513726.1:c.1989G>C
|
XP_011512028.1:p.Gln663His
|
|
XM_011513727.1:c.1989G>C
|
XP_011512029.1:p.Gln663His
|
|
XM_011513728.1:c.1977G>C
|
XP_011512030.1:p.Gln659His
|
|
XM_011513729.1:c.2469G>C
|
XP_011512031.1:p.Gln823His
|
|
XR_925155.1:n.2533G>C
|
|
|
NM_001317924.1:c.1977G>C
|
NP_001304853.1:p.Gln659His
|
|
XM_011513725.2:c.2403G>C
|
XP_011512027.1:p.Gln801His
|
|
XM_011513726.3:c.1989G>C
|
XP_011512028.1:p.Gln663His
|
|
XM_017008501.1:c.1977G>C
|
XP_016863990.1:p.Gln659His
|
|
XR_001741306.1:n.2533G>C
|
|
|
XR_001741307.1:n.2521G>C
|
|
|
XR_001741308.1:n.2533G>C
|
|
|
XR_001741309.1:n.2521G>C
|
|
|
XR_001741310.1:n.2521G>C
|
|
|
XR_001741311.2:n.2370G>C
|
|
|
NM_025132.4:c.2457G>C
MANE Select
|
NP_079408.3:p.Gln819His
|
|
NM_001317924.2:c.1977G>C
|
NP_001304853.1:p.Gln659His
|
|