ENST00000525083.6:n.775G>A
|
|
|
ENST00000532101.6:n.734-340G>A
|
|
|
ENST00000532125.2:c.594G>A
|
ENSP00000434178.2:p.Trp198Ter
|
|
ENST00000533839.6:c.86-807G>A
|
ENSP00000509952.1:n.86-807G>A
|
|
ENST00000534011.6:n.889G>A
|
|
|
ENST00000685484.1:c.597G>A
|
ENSP00000510622.1:p.Trp199Ter
|
|
ENST00000685601.1:c.597G>A
|
ENSP00000510603.1:p.Trp199Ter
|
|
ENST00000685765.1:c.597G>A
|
ENSP00000509991.1:p.Trp199Ter
|
|
ENST00000685844.1:c.*169-340G>A
|
ENSP00000509820.1:n.*169-340G>A
|
|
ENST00000685857.1:n.1031G>A
|
|
|
ENST00000686242.1:c.396G>A
|
ENSP00000508950.1:n.396G>A
|
|
ENST00000686888.1:c.*164G>A
|
ENSP00000509619.1:n.*164G>A
|
|
ENST00000687699.1:c.721G>A
|
ENSP00000508878.1:n.721G>A
|
|
ENST00000687786.1:n.2068-340G>A
|
|
|
ENST00000688100.1:n.1518G>A
|
|
|
ENST00000688588.1:c.597G>A
|
ENSP00000510802.1:p.Trp199Ter
|
|
ENST00000688927.1:n.2503G>A
|
|
|
ENST00000689283.1:c.*260G>A
|
ENSP00000509050.1:n.*260G>A
|
|
ENST00000689477.1:c.*490G>A
|
ENSP00000508945.1:n.*490G>A
|
|
ENST00000689765.1:c.*169-384G>A
|
ENSP00000509625.1:n.*169-384G>A
|
|
ENST00000690512.1:c.*448G>A
|
ENSP00000509793.1:n.*448G>A
|
|
ENST00000692039.1:c.*395G>A
|
ENSP00000508821.1:n.*395G>A
|
|
ENST00000692336.1:c.621G>A
|
ENSP00000508540.1:p.Trp207Ter
|
|
ENST00000693133.1:n.772G>A
|
|
|
ENST00000263578.10:c.597G>A
MANE Select
|
ENSP00000263578.5:p.Trp199Ter
|
|
ENST00000263578.9:c.597G>A
|
ENSP00000263578.5:p.Trp199Ter
|
|
ENST00000524751.5:n.533G>A
|
|
|
ENST00000525083.5:n.352-340G>A
|
|
|
ENST00000525770.5:c.*229G>A
|
ENSP00000434739.1:n.*229G>A
|
|
ENST00000526366.5:n.528G>A
|
|
|
ENST00000527004.5:c.534-340G>A
|
ENSP00000436374.1:n.534-340G>A
|
|
ENST00000527875.1:n.427G>A
|
|
|
ENST00000530642.1:n.1074G>A
|
|
|
ENST00000532101.5:n.820G>A
|
|
|
ENST00000532125.1:c.555G>A
|
ENSP00000434178.1:p.Trp185Ter
|
|
ENST00000533395.5:n.365-340G>A
|
|
|
ENST00000533839.5:n.238-807G>A
|
|
|
ENST00000534011.5:n.649G>A
|
|
|
ENST00000534315.5:n.944-340G>A
|
|
|
NM_017547.3:c.597G>A
|
NP_060017.1:p.Trp199Ter
|
|
NR_037647.1:n.543G>A
|
|
|
NR_037648.1:n.783G>A
|
|
|
XM_006718879.2:c.87G>A
|
XP_006718942.1:p.Trp29Ter
|
|
XM_006718880.2:c.-2-340G>A
|
XP_006718943.1:n.-2-340G>A
|
|
XM_006718881.2:c.-2-340G>A
|
XP_006718944.1:n.-2-340G>A
|
|
XM_011542895.1:c.87G>A
|
XP_011541197.1:p.Trp29Ter
|
|
XM_011542896.1:c.87G>A
|
XP_011541198.1:p.Trp29Ter
|
|
XM_006718879.3:c.87G>A
|
XP_006718942.1:p.Trp29Ter
|
|
XM_006718881.3:c.-2-340G>A
|
XP_006718944.1:n.-2-340G>A
|
|
XM_011542895.2:c.87G>A
|
XP_011541197.1:p.Trp29Ter
|
|
XM_011542896.2:c.87G>A
|
XP_011541198.1:p.Trp29Ter
|
|
XM_017018000.2:c.597G>A
|
XP_016873489.1:p.Trp199Ter
|
|
XM_017018001.1:c.87G>A
|
XP_016873490.1:p.Trp29Ter
|
|
XM_017018002.1:c.87G>A
|
XP_016873491.1:p.Trp29Ter
|
|
XM_017018003.2:c.-2-340G>A
|
XP_016873492.1:n.-2-340G>A
|
|
XM_017018004.1:c.-2-340G>A
|
XP_016873493.1:n.-2-340G>A
|
|
XM_017018005.1:c.-2-340G>A
|
XP_016873494.1:n.-2-340G>A
|
|
XM_017018006.2:c.-2-340G>A
|
XP_016873495.1:n.-2-340G>A
|
|
NM_017547.4:c.597G>A
MANE Select
|
NP_060017.1:p.Trp199Ter
|
|
NR_037647.2:n.429G>A
|
|
|
NR_037648.2:n.774G>A
|
|
|