ENST00000468029.2:c.229T>C
|
ENSP00000514912.1:p.Leu77=
|
|
ENST00000700275.1:c.229T>C
|
ENSP00000514910.1:p.Leu77=
|
|
ENST00000700276.1:c.139+2679T>C
|
ENSP00000514911.1:n.139+2679T>C
|
|
ENST00000700277.1:c.229T>C
|
ENSP00000514913.1:p.Leu77=
|
|
ENST00000700278.1:n.406T>C
|
|
|
ENST00000700279.1:n.487T>C
|
|
|
ENST00000296543.10:c.229T>C
MANE Select
|
ENSP00000296543.4:p.Leu77=
|
|
ENST00000296543.9:c.229T>C
|
ENSP00000296543.4:p.Leu77=
|
|
ENST00000398947.1:c.229T>C
|
ENSP00000381920.1:p.Leu77=
|
|
ENST00000480277.2:n.65T>C
|
|
|
ENST00000482087.1:n.373T>C
|
|
|
NM_057175.3:c.229T>C
|
NP_476516.1:p.Leu77=
|
|
XM_005263236.1:c.229T>C
|
XP_005263293.1:p.Leu77=
|
|
NM_057175.4:c.229T>C
|
NP_476516.1:p.Leu77=
|
|
XM_005263236.3:c.229T>C
|
XP_005263293.1:p.Leu77=
|
|
NM_057175.5:c.229T>C
MANE Select
|
NP_476516.1:p.Leu77=
|
|