|
ENST00000480961.3:n.986T>C
|
|
|
|
ENST00000484855.4:n.619T>C
|
|
|
|
ENST00000493522.8:n.597T>C
|
|
|
|
ENST00000606066.3:n.1060T>C
|
|
|
|
ENST00000606782.3:n.690T>C
|
|
|
|
ENST00000607187.3:n.986T>C
|
|
|
|
ENST00000607212.3:n.780T>C
|
|
|
|
ENST00000607814.7:n.1305T>C
|
|
|
|
ENST00000677755.2:n.989T>C
|
|
|
|
ENST00000678622.2:n.986T>C
|
|
|
|
ENST00000678691.2:n.986T>C
|
|
|
|
ENST00000678988.2:n.1608T>C
|
|
|
|
ENST00000679053.2:n.986T>C
|
|
|
|
ENST00000679343.2:n.986T>C
|
|
|
|
ENST00000684198.1:n.986T>C
|
|
|
|
ENST00000372459.7:c.569T>C
|
ENSP00000361537.2:p.Leu190Pro
|
|
|
ENST00000372484.8:c.623T>C
|
ENSP00000361562.3:p.Leu208Pro
|
|
|
ENST00000419493.3:c.569T>C
|
ENSP00000408533.3:p.Leu190Pro
|
|
|
ENST00000480961.2:n.596T>C
|
|
|
|
ENST00000484855.3:n.619T>C
|
|
|
|
ENST00000493522.7:n.597T>C
|
|
|
|
ENST00000606066.2:n.708T>C
|
|
|
|
ENST00000606394.6:c.*211T>C
|
ENSP00000475827.1:n.*211T>C
|
|
|
ENST00000606782.2:n.690T>C
|
|
|
|
ENST00000607187.2:n.500T>C
|
|
|
|
ENST00000607212.2:n.780T>C
|
|
|
|
ENST00000607482.6:c.569T>C
|
ENSP00000475524.2:p.Leu190Pro
|
|
|
ENST00000607814.6:n.1305T>C
|
|
|
|
ENST00000646241.3:c.569T>C
MANE Select
|
ENSP00000493613.2:p.Leu190Pro
|
|
|
ENST00000676526.1:c.623T>C
|
ENSP00000504209.1:p.Leu208Pro
|
|
|
ENST00000676597.1:c.569T>C
|
ENSP00000503904.1:p.Leu190Pro
|
|
|
ENST00000676657.1:c.569T>C
|
ENSP00000504158.1:p.Leu190Pro
|
|
|
ENST00000676967.1:c.569T>C
|
ENSP00000502866.1:p.Leu190Pro
|
|
|
ENST00000677394.1:c.623T>C
|
ENSP00000504790.1:p.Leu208Pro
|
|
|
ENST00000677525.1:c.*392T>C
|
ENSP00000504197.1:n.*392T>C
|
|
|
ENST00000677755.1:n.989T>C
|
|
|
|
ENST00000678025.1:c.569T>C
|
ENSP00000503463.1:p.Leu190Pro
|
|
|
ENST00000678078.1:c.623T>C
|
ENSP00000502993.1:p.Leu208Pro
|
|
|
ENST00000678217.1:c.569T>C
|
ENSP00000504109.1:p.Leu190Pro
|
|
|
ENST00000678331.1:c.569T>C
|
ENSP00000504524.1:p.Leu190Pro
|
|
|
ENST00000678443.1:c.569T>C
|
ENSP00000504006.1:p.Leu190Pro
|
|
|
ENST00000678512.1:n.833T>C
|
|
|
|
ENST00000678622.1:n.614T>C
|
|
|
|
ENST00000678691.1:n.447T>C
|
|
|
|
ENST00000678939.1:c.569T>C
|
ENSP00000503404.1:p.Leu190Pro
|
|
|
ENST00000678988.1:n.1608T>C
|
|
|
|
ENST00000679053.1:n.614T>C
|
|
|
|
ENST00000679343.1:n.607T>C
|
|
|
|
ENST00000191018.9:c.569T>C
|
ENSP00000191018.5:p.Leu190Pro
|
|
|
ENST00000354880.9:c.572T>C
|
ENSP00000346952.4:p.Leu191Pro
|
|
|
ENST00000372459.6:c.569T>C
|
ENSP00000361537.2:p.Leu190Pro
|
|
|
ENST00000372484.7:c.623T>C
|
ENSP00000361562.3:p.Leu208Pro
|
|
|
ENST00000419493.2:c.98T>C
|
ENSP00000408533.2:p.Leu33Pro
|
|
|
ENST00000485627.1:n.230T>C
|
|
|
|
ENST00000606394.5:c.*211T>C
|
ENSP00000475827.1:n.*211T>C
|
|
|
ENST00000606782.1:n.202T>C
|
|
|
|
ENST00000606788.5:c.623T>C
|
ENSP00000476235.1:p.Leu208Pro
|
|
|
NM_000308.2:c.623T>C
|
NP_000299.2:p.Leu208Pro
|
|
|
NM_000308.3:c.623T>C
|
NP_000299.2:p.Leu208Pro
|
|
|
NM_001127695.1:c.569T>C
|
NP_001121167.1:p.Leu190Pro
|
|
|
NM_001127695.2:c.569T>C
|
NP_001121167.1:p.Leu190Pro
|
|
|
NM_001167594.1:c.572T>C
|
NP_001161066.1:p.Leu191Pro
|
|
|
NM_001167594.2:c.572T>C
|
NP_001161066.1:p.Leu191Pro
|
|
|
NR_133656.1:n.1805T>C
|
|
|
|
NM_000308.4:c.569T>C
MANE Select
|
NP_000299.3:p.Leu190Pro
|
|
|
NM_001127695.3:c.569T>C
|
NP_001121167.1:p.Leu190Pro
|
|
|
NM_001167594.3:c.518T>C
|
NP_001161066.2:p.Leu173Pro
|
|
|
NR_133656.2:n.614T>C
|
|
|
