ENST00000700075.1:c.13T>A
|
ENSP00000514784.1:p.Trp5Arg
|
|
ENST00000342771.10:c.1945T>A
MANE Select
|
ENSP00000344087.4:p.Trp649Arg
|
|
ENST00000439256.2:c.43T>A
|
ENSP00000407058.2:p.Trp15Arg
|
|
ENST00000443672.2:c.280T>A
|
ENSP00000393548.2:p.Trp94Arg
|
|
ENST00000449547.6:c.38T>A
|
|
|
ENST00000464768.2:n.613T>A
|
|
|
ENST00000644359.1:c.526T>A
|
ENSP00000494561.1:p.Trp176Arg
|
|
ENST00000644506.1:c.571T>A
|
ENSP00000496672.1:p.Trp191Arg
|
|
ENST00000644939.1:c.1942T>A
|
ENSP00000496726.1:p.Trp648Arg
|
|
ENST00000644949.1:c.276T>A
|
|
|
ENST00000646136.1:n.256T>A
|
|
|
ENST00000647140.1:c.810T>A
|
|
|
ENST00000342771.8:c.1945T>A
|
ENSP00000344087.4:p.Trp649Arg
|
|
ENST00000406775.6:c.1873T>A
|
ENSP00000385263.2:p.Trp625Arg
|
|
ENST00000439256.1:c.43T>A
|
|
|
ENST00000443672.1:c.525T>A
|
|
|
ENST00000464768.1:n.611T>A
|
|
|
ENST00000465899.1:n.442T>A
|
|
|
ENST00000498384.5:n.313T>A
|
|
|
ENST00000611706.4:c.1201T>A
|
ENSP00000478134.1:p.Trp401Arg
|
|
ENST00000615871.4:c.1129T>A
|
ENSP00000479325.1:p.Trp377Arg
|
|
NM_001127231.2:c.1873T>A
|
NP_001120703.1:p.Trp625Arg
|
|
NM_015570.3:c.1945T>A
|
NP_056385.1:p.Trp649Arg
|
|
XM_005250257.1:c.592T>A
|
XP_005250314.1:p.Trp198Arg
|
|
XM_011516010.1:c.1966T>A
|
XP_011514312.1:p.Trp656Arg
|
|
XM_011516011.1:c.1963T>A
|
XP_011514313.1:p.Trp655Arg
|
|
XM_011516012.1:c.1900T>A
|
XP_011514314.1:p.Trp634Arg
|
|
XM_011516013.1:c.1894T>A
|
XP_011514315.1:p.Trp632Arg
|
|
XM_011516014.1:c.1864T>A
|
XP_011514316.1:p.Trp622Arg
|
|
XM_011516015.1:c.1702T>A
|
XP_011514317.1:p.Trp568Arg
|
|
XM_011516016.1:c.1675T>A
|
XP_011514318.1:p.Trp559Arg
|
|
XM_011516017.1:c.1492T>A
|
XP_011514319.1:p.Trp498Arg
|
|
XM_011516018.1:c.1465T>A
|
XP_011514320.1:p.Trp489Arg
|
|
XM_005250257.2:c.592T>A
|
XP_005250314.1:p.Trp198Arg
|
|
XM_011516010.2:c.1966T>A
|
XP_011514312.1:p.Trp656Arg
|
|
XM_011516011.2:c.1963T>A
|
XP_011514313.1:p.Trp655Arg
|
|
XM_011516012.2:c.1900T>A
|
XP_011514314.1:p.Trp634Arg
|
|
XM_011516013.2:c.1894T>A
|
XP_011514315.1:p.Trp632Arg
|
|
XM_011516014.2:c.1864T>A
|
XP_011514316.1:p.Trp622Arg
|
|
XM_011516017.2:c.1492T>A
|
XP_011514319.1:p.Trp498Arg
|
|
XM_011516018.2:c.1465T>A
|
XP_011514320.1:p.Trp489Arg
|
|
XM_017011951.2:c.1966T>A
|
XP_016867440.1:p.Trp656Arg
|
|
NM_001127231.3:c.1873T>A
|
NP_001120703.1:p.Trp625Arg
|
|
NM_015570.4:c.1945T>A
MANE Select
|
NP_056385.1:p.Trp649Arg
|
|