ENST00000540033.3:c.1882T>C
|
ENSP00000440826.2:p.Tyr628His
|
|
ENST00000706843.1:c.1873T>C
|
ENSP00000516584.1:p.Tyr625His
|
|
ENST00000706845.1:c.*1730T>C
|
ENSP00000516587.1:n.*1730T>C
|
|
ENST00000706846.1:c.1897T>C
|
ENSP00000516588.1:p.Tyr633His
|
|
ENST00000706867.1:c.1978T>C
|
ENSP00000516594.1:p.Tyr660His
|
|
ENST00000706868.1:c.1897T>C
|
ENSP00000516595.1:p.Tyr633His
|
|
ENST00000706869.1:n.310-3859T>C
|
|
|
ENST00000706883.1:c.685T>C
|
ENSP00000516600.1:p.Tyr229His
|
|
ENST00000706885.1:c.1762T>C
|
ENSP00000516601.1:p.Tyr588His
|
|
ENST00000684568.2:c.1897T>C
MANE Select
|
ENSP00000506999.1:p.Tyr633His
|
|
ENST00000370331.5:c.1849T>C
|
ENSP00000359356.1:p.Tyr617His
|
|
ENST00000468580.5:n.612T>C
|
|
|
ENST00000491940.5:n.702T>C
|
|
|
ENST00000492513.5:n.370T>C
|
|
|
ENST00000540033.2:c.1882T>C
|
ENSP00000440826.2:p.Tyr628His
|
|
NM_001308248.1:c.1882T>C
|
NP_001295177.1:p.Tyr628His
|
|
NM_005665.4:c.1849T>C
|
NP_005656.4:p.Tyr617His
|
|
NM_005665.5:c.1849T>C
|
NP_005656.4:p.Tyr617His
|
|
XM_011542099.1:c.2101T>C
|
XP_011540401.1:p.Tyr701His
|
|
XM_011542100.1:c.2101T>C
|
XP_011540402.1:p.Tyr701His
|
|
XM_011542101.1:c.1978T>C
|
XP_011540403.1:p.Tyr660His
|
|
XM_011542102.1:c.1954T>C
|
XP_011540404.1:p.Tyr652His
|
|
XM_011542103.1:c.2032-2256T>C
|
XP_011540405.1:n.2032-2256T>C
|
|
XM_011542104.1:c.1942T>C
|
XP_011540406.1:p.Tyr648His
|
|
XM_011542105.1:c.1921T>C
|
XP_011540407.1:p.Tyr641His
|
|
XM_011542107.1:c.1849T>C
|
XP_011540409.1:p.Tyr617His
|
|
XM_011542108.1:c.2101T>C
|
XP_011540410.1:p.Tyr701His
|
|
XM_011542109.1:c.2101T>C
|
XP_011540411.1:p.Tyr701His
|
|
NM_001350197.1:c.1897T>C
|
NP_001337126.1:p.Tyr633His
|
|
NM_001350198.1:c.1897T>C
|
NP_001337127.1:p.Tyr633His
|
|
XM_017002269.1:c.2110T>C
|
XP_016857758.1:p.Tyr704His
|
|
XM_017002270.2:c.2101T>C
|
XP_016857759.1:p.Tyr701His
|
|
XM_017002271.2:c.2029T>C
|
XP_016857760.1:p.Tyr677His
|
|
XM_017002272.1:c.2110T>C
|
XP_016857761.1:p.Tyr704His
|
|
XM_017002273.2:c.1978T>C
|
XP_016857762.1:p.Tyr660His
|
|
XM_017002274.1:c.1978T>C
|
XP_016857763.1:p.Tyr660His
|
|
XM_017002275.1:c.1978T>C
|
XP_016857764.1:p.Tyr660His
|
|
XM_017002276.2:c.1897T>C
|
XP_016857765.1:p.Tyr633His
|
|
XM_017002277.1:c.1882T>C
|
XP_016857766.1:p.Tyr628His
|
|
XM_017002278.1:c.1963T>C
|
XP_016857767.1:p.Tyr655His
|
|
XM_017002279.1:c.1843T>C
|
XP_016857768.1:p.Tyr615His
|
|
XM_017002281.2:c.1873T>C
|
XP_016857770.1:p.Tyr625His
|
|
XM_017002282.1:c.2110T>C
|
XP_016857771.1:p.Tyr704His
|
|
XM_017002283.1:c.2029T>C
|
XP_016857772.1:p.Tyr677His
|
|
XM_017002284.2:c.1750T>C
|
XP_016857773.1:p.Tyr584His
|
|
XM_017002286.2:c.1486T>C
|
XP_016857775.1:p.Tyr496His
|
|
XM_017002287.2:c.1486T>C
|
XP_016857776.1:p.Tyr496His
|
|
XM_017002288.1:c.1486T>C
|
XP_016857777.1:p.Tyr496His
|
|
XM_024449686.1:c.2029T>C
|
XP_024305454.1:p.Tyr677His
|
|
XM_024449689.1:c.1930T>C
|
XP_024305457.1:p.Tyr644His
|
|
XM_024449690.1:c.1762T>C
|
XP_024305458.1:p.Tyr588His
|
|
NM_001308248.2:c.1882T>C
|
NP_001295177.1:p.Tyr628His
|
|
NM_001350197.2:c.1897T>C
MANE Select
|
NP_001337126.1:p.Tyr633His
|
|
NM_001350198.2:c.1897T>C
|
NP_001337127.1:p.Tyr633His
|
|
NM_001377210.1:c.1873T>C
|
NP_001364139.1:p.Tyr625His
|
|
NM_001377211.1:c.1855T>C
|
NP_001364140.1:p.Tyr619His
|
|
NM_001377212.1:c.1750T>C
|
NP_001364141.1:p.Tyr584His
|
|
NM_001377213.1:c.1978T>C
|
NP_001364142.1:p.Tyr660His
|
|
NM_005665.6:c.1849T>C
|
NP_005656.4:p.Tyr617His
|
|