ENST00000481478.2:c.6470A>T
|
ENSP00000418014.2:p.Tyr2157Phe
|
|
ENST00000636581.2:n.1799A>T
|
|
|
ENST00000636633.2:n.3409A>T
|
|
|
ENST00000636999.2:n.1845A>T
|
|
|
ENST00000288139.11:c.6470A>T
MANE Plus Clinical
|
ENSP00000288139.3:p.Tyr2157Phe
|
|
ENST00000350061.11:c.6410A>T
MANE Select
|
ENSP00000288133.5:p.Tyr2137Phe
|
|
ENST00000422281.7:c.6338A>T
|
ENSP00000409174.2:p.Tyr2113Phe
|
|
ENST00000636448.1:c.2531A>T
|
|
|
ENST00000636570.1:c.6365A>T
|
ENSP00000490183.1:p.Tyr2122Phe
|
|
ENST00000636581.1:n.1799A>T
|
|
|
ENST00000636633.1:n.3409A>T
|
|
|
ENST00000636999.1:n.1837A>T
|
|
|
ENST00000637424.1:c.6437A>T
|
ENSP00000489769.1:p.Tyr2146Phe
|
|
ENST00000288139.8:c.6470A>T
|
ENSP00000288139.3:p.Tyr2157Phe
|
|
ENST00000350061.9:c.6410A>T
|
ENSP00000288133.5:p.Tyr2137Phe
|
|
ENST00000422281.6:c.6338A>T
|
ENSP00000409174.2:p.Tyr2113Phe
|
|
ENST00000481478.1:c.5489A>T
|
ENSP00000418014.1:p.Tyr1830Phe
|
|
NM_000720.3:c.6470A>T
|
NP_000711.1:p.Tyr2157Phe
|
|
NM_001128839.2:c.6338A>T
|
NP_001122311.1:p.Tyr2113Phe
|
|
NM_001128840.2:c.6410A>T
|
NP_001122312.1:p.Tyr2137Phe
|
|
XM_005265448.2:c.6365A>T
|
XP_005265505.1:p.Tyr2122Phe
|
|
XM_011534094.1:c.6665A>T
|
XP_011532396.1:p.Tyr2222Phe
|
|
XM_011534095.1:c.6554A>T
|
XP_011532397.1:p.Tyr2185Phe
|
|
XM_011534096.1:c.6476A>T
|
XP_011532398.1:p.Tyr2159Phe
|
|
XM_011534097.1:c.6128A>T
|
XP_011532399.1:p.Tyr2043Phe
|
|
XM_011534098.1:c.6128A>T
|
XP_011532400.1:p.Tyr2043Phe
|
|
XM_011534099.1:c.5753A>T
|
XP_011532401.1:p.Tyr1918Phe
|
|
XM_011534100.1:c.6560A>T
|
XP_011532402.1:p.Tyr2187Phe
|
|
XM_005265448.3:c.6365A>T
|
XP_005265505.1:p.Tyr2122Phe
|
|
XM_011534094.2:c.6665A>T
|
XP_011532396.1:p.Tyr2222Phe
|
|
XM_011534096.2:c.6476A>T
|
XP_011532398.1:p.Tyr2159Phe
|
|
XM_011534097.2:c.6128A>T
|
XP_011532399.1:p.Tyr2043Phe
|
|
XM_011534099.2:c.5753A>T
|
XP_011532401.1:p.Tyr1918Phe
|
|
XM_011534100.2:c.6560A>T
|
XP_011532402.1:p.Tyr2187Phe
|
|
XM_017007137.1:c.6665A>T
|
XP_016862626.1:p.Tyr2222Phe
|
|
XM_017007138.1:c.6662A>T
|
XP_016862627.1:p.Tyr2221Phe
|
|
XM_017007139.1:c.6638A>T
|
XP_016862628.1:p.Tyr2213Phe
|
|
XM_017007140.1:c.6605A>T
|
XP_016862629.1:p.Tyr2202Phe
|
|
XM_017007141.1:c.6605A>T
|
XP_016862630.1:p.Tyr2202Phe
|
|
XM_017007142.1:c.6581A>T
|
XP_016862631.1:p.Tyr2194Phe
|
|
XM_017007143.1:c.6581A>T
|
XP_016862632.1:p.Tyr2194Phe
|
|
XM_017007144.1:c.6581A>T
|
XP_016862633.1:p.Tyr2194Phe
|
|
XM_017007145.1:c.6536A>T
|
XP_016862634.1:p.Tyr2179Phe
|
|
NM_001128840.3:c.6410A>T
MANE Select
|
NP_001122312.1:p.Tyr2137Phe
|
|
NM_000720.4:c.6470A>T
MANE Plus Clinical
|
NP_000711.1:p.Tyr2157Phe
|
|
NM_001128839.3:c.6338A>T
|
NP_001122311.1:p.Tyr2113Phe
|
|