ENST00000255078.8:c.919A>C
MANE Select
|
ENSP00000255078.4:p.Asn307His
|
|
ENST00000539224.2:c.1048A>C
|
|
|
ENST00000674745.1:c.7A>C
|
ENSP00000502738.1:p.Asn3His
|
|
ENST00000674775.1:n.7A>C
|
|
|
ENST00000674955.1:c.919A>C
|
ENSP00000502463.1:p.Asn307His
|
|
ENST00000675118.1:c.407A>C
|
|
|
ENST00000675119.1:c.346A>C
|
ENSP00000501861.1:n.346A>C
|
|
ENST00000675305.1:c.239A>C
|
ENSP00000502365.1:n.239A>C
|
|
ENST00000675464.1:c.202A>C
|
ENSP00000502650.1:p.Asn68His
|
|
ENST00000675493.1:n.7A>C
|
|
|
ENST00000675615.1:c.919A>C
|
ENSP00000502413.1:p.Asn307His
|
|
ENST00000675648.1:n.294A>C
|
|
|
ENST00000675683.1:c.306A>C
|
|
|
ENST00000675684.1:c.7A>C
|
ENSP00000502192.1:p.Asn3His
|
|
ENST00000676173.1:n.963A>C
|
|
|
ENST00000676228.1:c.*242A>C
|
ENSP00000502375.1:n.*242A>C
|
|
ENST00000255078.7:c.919A>C
|
ENSP00000255078.3:p.Asn307His
|
|
NM_002180.2:c.919A>C , LRG_250t1:c.919A>C
|
NP_002171.2:p.Asn307His
|
|
XM_005273974.2:c.-93A>C
|
XP_005274031.1:n.-93A>C
|
|
XM_005273976.1:c.919A>C
|
XP_005274033.1:p.Asn307His
|
|
XR_247198.1:n.1021A>C
|
|
|
XR_949903.1:n.1021A>C
|
|
|
XM_005273976.2:c.919A>C
|
XP_005274033.1:p.Asn307His
|
|
XM_017017669.2:c.-93A>C
|
XP_016873158.1:n.-93A>C
|
|
XM_017017670.2:c.-93A>C
|
XP_016873159.1:n.-93A>C
|
|
XM_017017671.2:c.919A>C
|
XP_016873160.1:p.Asn307His
|
|
XR_949903.3:n.1017A>C
|
|
|
NM_002180.3:c.919A>C
MANE Select
|
NP_002171.2:p.Asn307His
|
|