ENST00000269321.12:c.355A>C
MANE Select
|
ENSP00000269321.7:p.Asn119His
|
|
ENST00000269321.11:c.355A>C
|
ENSP00000269321.7:p.Asn119His
|
|
ENST00000400721.8:c.355A>C
|
ENSP00000383556.4:p.Asn119His
|
|
ENST00000541078.6:c.355A>C
|
ENSP00000441348.2:p.Asn119His
|
|
ENST00000578351.1:c.278A>C
|
ENSP00000462323.1:p.Ter93Ser
|
|
ENST00000579121.5:c.355A>C
|
ENSP00000462960.1:p.Asn119His
|
|
ENST00000580033.5:c.278A>C
|
ENSP00000463530.1:p.Ter93Ser
|
|
ENST00000580685.5:c.355A>C
|
ENSP00000464205.1:p.Asn119His
|
|
ENST00000581876.5:c.191-158A>C
|
ENSP00000461956.1:n.191-158A>C
|
|
ENST00000582984.5:n.557A>C
|
|
|
ENST00000583111.5:n.507A>C
|
|
|
ENST00000583791.1:n.219A>C
|
|
|
ENST00000583868.5:c.355A>C
|
ENSP00000462209.1:p.Asn119His
|
|
ENST00000584461.5:c.355A>C
|
ENSP00000463939.1:p.Asn119His
|
|
NM_001185077.2:c.355A>C
|
NP_001172006.1:p.Asn119His
|
|
NM_001185078.2:c.355A>C
|
NP_001172007.1:p.Asn119His
|
|
NM_001301240.1:c.355A>C
|
NP_001288169.1:p.Asn119His
|
|
NM_001301241.1:c.355A>C
|
NP_001288170.1:p.Asn119His
|
|
NM_001301242.1:c.355A>C
|
NP_001288171.1:p.Asn119His
|
|
NM_001301243.1:c.490A>C
|
NP_001288172.1:p.Asn164His
|
|
NM_004309.5:c.355A>C
|
NP_004300.1:p.Asn119His
|
|
NR_125441.1:n.414A>C
|
|
|
XM_011523574.1:c.490A>C
|
XP_011521876.1:p.Asn164His
|
|
NM_004309.6:c.355A>C
MANE Select
|
NP_004300.1:p.Asn119His
|
|
NM_001185077.3:c.355A>C
|
NP_001172006.1:p.Asn119His
|
|
NM_001185078.3:c.355A>C
|
NP_001172007.1:p.Asn119His
|
|
NM_001301240.2:c.355A>C
|
NP_001288169.1:p.Asn119His
|
|
NM_001301241.2:c.355A>C
|
NP_001288170.1:p.Asn119His
|
|
NM_001301242.2:c.355A>C
|
NP_001288171.1:p.Asn119His
|
|
NM_001301243.2:c.490A>C
|
NP_001288172.1:p.Asn164His
|
|
NR_125441.2:n.345A>C
|
|
|