ENST00000682089.1:n.521T>A
|
|
|
ENST00000682266.1:c.751T>A
|
ENSP00000507766.1:p.Trp251Arg
|
|
ENST00000682341.1:c.1159T>A
|
ENSP00000508251.1:p.Trp387Arg
|
|
ENST00000682530.1:c.*1133T>A
|
ENSP00000506805.1:n.*1133T>A
|
|
ENST00000683197.1:c.1159T>A
|
ENSP00000507641.1:p.Trp387Arg
|
|
ENST00000683411.1:c.751T>A
|
ENSP00000508397.1:p.Trp251Arg
|
|
ENST00000683437.1:c.751T>A
|
ENSP00000508408.1:p.Trp251Arg
|
|
ENST00000683613.1:n.2195T>A
|
|
|
ENST00000683834.1:n.1401T>A
|
|
|
ENST00000684663.1:c.1156T>A
|
ENSP00000508009.1:p.Trp386Arg
|
|
ENST00000324559.9:c.1201T>A
MANE Select
|
ENSP00000315371.9:p.Trp401Arg
|
|
ENST00000648804.1:n.1536T>A
|
|
|
ENST00000324559.8:c.1201T>A
|
ENSP00000315371.8:p.Trp401Arg
|
|
NM_001142649.1:c.1198T>A
|
NP_001136121.1:p.Trp400Arg
|
|
NM_213599.2:c.1201T>A , LRG_868t1:c.1201T>A
|
NP_998764.1:p.Trp401Arg
|
|
XM_005252820.2:c.1159T>A
|
XP_005252877.2:p.Trp387Arg
|
|
XM_005252821.2:c.1156T>A
|
XP_005252878.2:p.Trp386Arg
|
|
XM_005252822.3:c.1123T>A
|
XP_005252879.1:p.Trp375Arg
|
|
XM_005252823.3:c.1120T>A
|
XP_005252880.1:p.Trp374Arg
|
|
XM_011519949.1:c.1108T>A
|
XP_011518251.1:p.Trp370Arg
|
|
XM_005252820.3:c.1159T>A
|
XP_005252877.2:p.Trp387Arg
|
|
XM_005252821.3:c.1156T>A
|
XP_005252878.2:p.Trp386Arg
|
|
XM_005252822.4:c.1123T>A
|
XP_005252879.1:p.Trp375Arg
|
|
XM_011519949.2:c.1108T>A
|
XP_011518251.1:p.Trp370Arg
|
|
NM_001142649.2:c.1198T>A
|
NP_001136121.1:p.Trp400Arg
|
|
NM_213599.3:c.1201T>A
MANE Select
|
NP_998764.1:p.Trp401Arg
|
|