ENST00000261304.7:c.219T>C
MANE Select
|
ENSP00000261304.2:p.Asn73=
|
|
ENST00000261304.6:c.219T>C
|
ENSP00000261304.2:p.Asn73=
|
|
ENST00000393568.8:c.196-293T>C
|
ENSP00000377198.4:n.196-293T>C
|
|
ENST00000393569.6:c.141T>C
|
ENSP00000377199.2:p.Asn47=
|
|
ENST00000474294.6:n.209T>C
|
|
|
ENST00000544807.6:c.51T>C
|
ENSP00000437513.2:p.Asn17=
|
|
ENST00000554372.5:c.219T>C
|
ENSP00000451884.1:p.Asn73=
|
|
ENST00000554916.5:n.98T>C
|
|
|
ENST00000555956.1:n.24T>C
|
|
|
ENST00000556879.5:c.279T>C
|
ENSP00000452208.1:n.279T>C
|
|
ENST00000557316.5:c.219T>C
|
ENSP00000452314.1:p.Asn73=
|
|
ENST00000622264.4:c.209T>C
|
|
|
NM_000153.3:c.219T>C
|
NP_000144.2:p.Asn73=
|
|
NM_001201401.1:c.196-293T>C
|
NP_001188330.1:n.196-293T>C
|
|
NM_001201402.1:c.141T>C
|
NP_001188331.1:p.Asn47=
|
|
XM_011536618.1:c.51T>C
|
XP_011534920.1:p.Asn17=
|
|
XM_011536618.2:c.51T>C
|
XP_011534920.1:p.Asn17=
|
|
NM_000153.4:c.219T>C
MANE Select
|
NP_000144.2:p.Asn73=
|
|
NM_001201401.2:c.196-293T>C
|
NP_001188330.1:n.196-293T>C
|
|
NM_001201402.2:c.141T>C
|
NP_001188331.1:p.Asn47=
|
|