ENST00000481478.2:c.5462T>C
|
ENSP00000418014.2:p.Val1821Ala
|
|
ENST00000636633.2:n.2401T>C
|
|
|
ENST00000636999.2:n.837T>C
|
|
|
ENST00000288139.11:c.5462T>C
MANE Plus Clinical
|
ENSP00000288139.3:p.Val1821Ala
|
|
ENST00000350061.11:c.5402T>C
MANE Select
|
ENSP00000288133.5:p.Val1801Ala
|
|
ENST00000422281.7:c.5357T>C
|
ENSP00000409174.2:p.Val1786Ala
|
|
ENST00000636448.1:c.1523T>C
|
|
|
ENST00000636570.1:c.5357T>C
|
ENSP00000490183.1:p.Val1786Ala
|
|
ENST00000636629.1:n.758T>C
|
|
|
ENST00000636633.1:n.2401T>C
|
|
|
ENST00000636999.1:n.829T>C
|
|
|
ENST00000637424.1:c.5429T>C
|
ENSP00000489769.1:p.Val1810Ala
|
|
ENST00000637844.1:n.156T>C
|
|
|
ENST00000288139.8:c.5462T>C
|
ENSP00000288139.3:p.Val1821Ala
|
|
ENST00000350061.9:c.5402T>C
|
ENSP00000288133.5:p.Val1801Ala
|
|
ENST00000422281.6:c.5357T>C
|
ENSP00000409174.2:p.Val1786Ala
|
|
ENST00000481478.1:c.4481T>C
|
ENSP00000418014.1:p.Val1494Ala
|
|
NM_000720.3:c.5462T>C
|
NP_000711.1:p.Val1821Ala
|
|
NM_001128839.2:c.5357T>C
|
NP_001122311.1:p.Val1786Ala
|
|
NM_001128840.2:c.5402T>C
|
NP_001122312.1:p.Val1801Ala
|
|
XM_005265448.2:c.5357T>C
|
XP_005265505.1:p.Val1786Ala
|
|
XM_011534094.1:c.5657T>C
|
XP_011532396.1:p.Val1886Ala
|
|
XM_011534095.1:c.5546T>C
|
XP_011532397.1:p.Val1849Ala
|
|
XM_011534096.1:c.5468T>C
|
XP_011532398.1:p.Val1823Ala
|
|
XM_011534097.1:c.5120T>C
|
XP_011532399.1:p.Val1707Ala
|
|
XM_011534098.1:c.5120T>C
|
XP_011532400.1:p.Val1707Ala
|
|
XM_011534099.1:c.4745T>C
|
XP_011532401.1:p.Val1582Ala
|
|
XM_011534100.1:c.5552T>C
|
XP_011532402.1:p.Val1851Ala
|
|
XM_005265448.3:c.5357T>C
|
XP_005265505.1:p.Val1786Ala
|
|
XM_011534094.2:c.5657T>C
|
XP_011532396.1:p.Val1886Ala
|
|
XM_011534096.2:c.5468T>C
|
XP_011532398.1:p.Val1823Ala
|
|
XM_011534097.2:c.5120T>C
|
XP_011532399.1:p.Val1707Ala
|
|
XM_011534099.2:c.4745T>C
|
XP_011532401.1:p.Val1582Ala
|
|
XM_011534100.2:c.5552T>C
|
XP_011532402.1:p.Val1851Ala
|
|
XM_017007137.1:c.5657T>C
|
XP_016862626.1:p.Val1886Ala
|
|
XM_017007138.1:c.5654T>C
|
XP_016862627.1:p.Val1885Ala
|
|
XM_017007139.1:c.5657T>C
|
XP_016862628.1:p.Val1886Ala
|
|
XM_017007140.1:c.5597T>C
|
XP_016862629.1:p.Val1866Ala
|
|
XM_017007141.1:c.5597T>C
|
XP_016862630.1:p.Val1866Ala
|
|
XM_017007142.1:c.5573T>C
|
XP_016862631.1:p.Val1858Ala
|
|
XM_017007143.1:c.5573T>C
|
XP_016862632.1:p.Val1858Ala
|
|
XM_017007144.1:c.5573T>C
|
XP_016862633.1:p.Val1858Ala
|
|
XM_017007145.1:c.5528T>C
|
XP_016862634.1:p.Val1843Ala
|
|
NM_001128840.3:c.5402T>C
MANE Select
|
NP_001122312.1:p.Val1801Ala
|
|
NM_000720.4:c.5462T>C
MANE Plus Clinical
|
NP_000711.1:p.Val1821Ala
|
|
NM_001128839.3:c.5357T>C
|
NP_001122311.1:p.Val1786Ala
|
|