|
ENST00000700075.1:c.41G>A
|
ENSP00000514784.1:p.Trp14Ter
|
|
|
ENST00000342771.10:c.1973G>A
MANE Select
|
ENSP00000344087.4:p.Trp658Ter
|
|
|
ENST00000439256.2:c.71G>A
|
ENSP00000407058.2:p.Trp24Ter
|
|
|
ENST00000443672.2:c.308G>A
|
ENSP00000393548.2:p.Trp103Ter
|
|
|
ENST00000449547.6:c.66G>A
|
|
|
|
ENST00000464768.2:n.641G>A
|
|
|
|
ENST00000644359.1:c.554G>A
|
ENSP00000494561.1:p.Trp185Ter
|
|
|
ENST00000644506.1:c.599G>A
|
ENSP00000496672.1:p.Trp200Ter
|
|
|
ENST00000644939.1:c.1970G>A
|
ENSP00000496726.1:p.Trp657Ter
|
|
|
ENST00000646136.1:n.284G>A
|
|
|
|
ENST00000647140.1:c.838G>A
|
|
|
|
ENST00000342771.8:c.1973G>A
|
ENSP00000344087.4:p.Trp658Ter
|
|
|
ENST00000406775.6:c.1901G>A
|
ENSP00000385263.2:p.Trp634Ter
|
|
|
ENST00000439256.1:c.71G>A
|
|
|
|
ENST00000464768.1:n.639G>A
|
|
|
|
ENST00000465899.1:n.470G>A
|
|
|
|
ENST00000498384.5:n.341G>A
|
|
|
|
ENST00000611706.4:c.1229G>A
|
ENSP00000478134.1:p.Trp410Ter
|
|
|
ENST00000615871.4:c.1157G>A
|
ENSP00000479325.1:p.Trp386Ter
|
|
|
NM_001127231.2:c.1901G>A
|
NP_001120703.1:p.Trp634Ter
|
|
|
NM_015570.3:c.1973G>A
|
NP_056385.1:p.Trp658Ter
|
|
|
XM_005250257.1:c.620G>A
|
XP_005250314.1:p.Trp207Ter
|
|
|
XM_011516010.1:c.1994G>A
|
XP_011514312.1:p.Trp665Ter
|
|
|
XM_011516011.1:c.1991G>A
|
XP_011514313.1:p.Trp664Ter
|
|
|
XM_011516012.1:c.1928G>A
|
XP_011514314.1:p.Trp643Ter
|
|
|
XM_011516013.1:c.1922G>A
|
XP_011514315.1:p.Trp641Ter
|
|
|
XM_011516014.1:c.1892G>A
|
XP_011514316.1:p.Trp631Ter
|
|
|
XM_011516015.1:c.1730G>A
|
XP_011514317.1:p.Trp577Ter
|
|
|
XM_011516016.1:c.1703G>A
|
XP_011514318.1:p.Trp568Ter
|
|
|
XM_011516017.1:c.1520G>A
|
XP_011514319.1:p.Trp507Ter
|
|
|
XM_011516018.1:c.1493G>A
|
XP_011514320.1:p.Trp498Ter
|
|
|
XM_005250257.2:c.620G>A
|
XP_005250314.1:p.Trp207Ter
|
|
|
XM_011516010.2:c.1994G>A
|
XP_011514312.1:p.Trp665Ter
|
|
|
XM_011516011.2:c.1991G>A
|
XP_011514313.1:p.Trp664Ter
|
|
|
XM_011516012.2:c.1928G>A
|
XP_011514314.1:p.Trp643Ter
|
|
|
XM_011516013.2:c.1922G>A
|
XP_011514315.1:p.Trp641Ter
|
|
|
XM_011516014.2:c.1892G>A
|
XP_011514316.1:p.Trp631Ter
|
|
|
XM_011516017.2:c.1520G>A
|
XP_011514319.1:p.Trp507Ter
|
|
|
XM_011516018.2:c.1493G>A
|
XP_011514320.1:p.Trp498Ter
|
|
|
XM_017011951.2:c.1994G>A
|
XP_016867440.1:p.Trp665Ter
|
|
|
NM_001127231.3:c.1901G>A
|
NP_001120703.1:p.Trp634Ter
|
|
|
NM_015570.4:c.1973G>A
MANE Select
|
NP_056385.1:p.Trp658Ter
|
|
