ENST00000399820.8:c.2460G>C
MANE Select
|
ENSP00000382717.3:p.Met820Ile
|
|
ENST00000399820.7:c.2460G>C
|
ENSP00000382717.3:p.Met820Ile
|
|
ENST00000506869.5:c.*2041G>C
|
ENSP00000424319.1:n.*2041G>C
|
|
ENST00000512095.5:n.1458G>C
|
|
|
NM_025132.3:c.2460G>C
|
NP_079408.3:p.Met820Ile
|
|
XM_011513724.1:c.2472G>C
|
XP_011512026.1:p.Met824Ile
|
|
XM_011513725.1:c.2406G>C
|
XP_011512027.1:p.Met802Ile
|
|
XM_011513726.1:c.1992G>C
|
XP_011512028.1:p.Met664Ile
|
|
XM_011513727.1:c.1992G>C
|
XP_011512029.1:p.Met664Ile
|
|
XM_011513728.1:c.1980G>C
|
XP_011512030.1:p.Met660Ile
|
|
XM_011513729.1:c.2472G>C
|
XP_011512031.1:p.Met824Ile
|
|
XR_925155.1:n.2536G>C
|
|
|
NM_001317924.1:c.1980G>C
|
NP_001304853.1:p.Met660Ile
|
|
XM_011513725.2:c.2406G>C
|
XP_011512027.1:p.Met802Ile
|
|
XM_011513726.3:c.1992G>C
|
XP_011512028.1:p.Met664Ile
|
|
XM_017008501.1:c.1980G>C
|
XP_016863990.1:p.Met660Ile
|
|
XR_001741306.1:n.2536G>C
|
|
|
XR_001741307.1:n.2524G>C
|
|
|
XR_001741308.1:n.2536G>C
|
|
|
XR_001741309.1:n.2524G>C
|
|
|
XR_001741310.1:n.2524G>C
|
|
|
XR_001741311.2:n.2373G>C
|
|
|
NM_025132.4:c.2460G>C
MANE Select
|
NP_079408.3:p.Met820Ile
|
|
NM_001317924.2:c.1980G>C
|
NP_001304853.1:p.Met660Ile
|
|