ENST00000265838.9:c.1048T>C
MANE Select
|
ENSP00000265838.4:p.Trp350Arg
|
|
ENST00000671707.1:n.1143T>C
|
|
|
ENST00000672031.1:c.*35T>C
|
ENSP00000500463.1:n.*35T>C
|
|
ENST00000672284.1:c.778T>C
|
ENSP00000500444.1:p.Trp260Arg
|
|
ENST00000672354.1:c.1048T>C
|
ENSP00000500490.1:p.Trp350Arg
|
|
ENST00000672367.1:c.685T>C
|
ENSP00000500209.1:p.Trp229Arg
|
|
ENST00000672580.1:c.*303T>C
|
ENSP00000500366.1:n.*303T>C
|
|
ENST00000672907.1:c.733T>C
|
ENSP00000500928.1:p.Trp245Arg
|
|
ENST00000673000.1:n.1136T>C
|
|
|
ENST00000673531.1:c.778T>C
|
ENSP00000500163.1:p.Trp260Arg
|
|
ENST00000265838.8:c.1048T>C
|
ENSP00000265838.4:p.Trp350Arg
|
|
ENST00000533597.1:n.124T>C
|
|
|
NM_000019.3:c.1048T>C
|
NP_000010.1:p.Trp350Arg
|
|
XM_006718834.2:c.778T>C
|
XP_006718897.1:p.Trp260Arg
|
|
XM_006718835.2:c.778T>C
|
XP_006718898.1:p.Trp260Arg
|
|
XM_006718835.3:c.778T>C
|
XP_006718898.1:p.Trp260Arg
|
|
XM_017017681.1:c.778T>C
|
XP_016873170.1:p.Trp260Arg
|
|
XM_017017682.2:c.670T>C
|
XP_016873171.1:p.Trp224Arg
|
|
XM_017017683.2:c.670T>C
|
XP_016873172.1:p.Trp224Arg
|
|
XM_024448511.1:c.778T>C
|
XP_024304279.1:p.Trp260Arg
|
|
XM_024448512.1:c.778T>C
|
XP_024304280.1:p.Trp260Arg
|
|
XM_024448513.1:c.778T>C
|
XP_024304281.1:p.Trp260Arg
|
|
XM_024448514.1:c.778T>C
|
XP_024304282.1:p.Trp260Arg
|
|
XM_024448515.1:c.778T>C
|
XP_024304283.1:p.Trp260Arg
|
|
NM_000019.4:c.1048T>C
MANE Select
|
NP_000010.1:p.Trp350Arg
|
|
NM_001386677.1:c.1048T>C
|
NP_001373606.1:p.Trp350Arg
|
|
NM_001386678.1:c.733T>C
|
NP_001373607.1:p.Trp245Arg
|
|
NM_001386679.1:c.751T>C
|
NP_001373608.1:p.Trp251Arg
|
|
NM_001386681.1:c.778T>C
|
NP_001373610.1:p.Trp260Arg
|
|
NM_001386682.1:c.778T>C
|
NP_001373611.1:p.Trp260Arg
|
|
NM_001386685.1:c.778T>C
|
NP_001373614.1:p.Trp260Arg
|
|
NM_001386686.1:c.778T>C
|
NP_001373615.1:p.Trp260Arg
|
|
NM_001386687.1:c.778T>C
|
NP_001373616.1:p.Trp260Arg
|
|
NM_001386688.1:c.778T>C
|
NP_001373617.1:p.Trp260Arg
|
|
NM_001386689.1:c.778T>C
|
NP_001373618.1:p.Trp260Arg
|
|
NM_001386690.1:c.778T>C
|
NP_001373619.1:p.Trp260Arg
|
|
NM_001386691.1:c.778T>C
|
NP_001373620.1:p.Trp260Arg
|
|
NR_170162.1:n.1023T>C
|
|
|
NR_170163.1:n.1081T>C
|
|
|