ENST00000698238.1:c.563G>A
|
ENSP00000513620.1:p.Arg188Lys
|
|
ENST00000476941.6:c.254G>A
MANE Select
|
ENSP00000419313.1:p.Arg85Lys
|
|
ENST00000273482.10:c.254G>A
|
ENSP00000273482.6:p.Arg85Lys
|
|
ENST00000460401.1:c.167+11729G>A
|
|
|
ENST00000476941.5:c.254G>A
|
ENSP00000419313.1:p.Arg85Lys
|
|
ENST00000612385.1:c.254G>A
|
ENSP00000481537.1:p.Arg85Lys
|
|
NM_001251845.1:c.254G>A
|
NP_001238774.1:p.Arg85Lys
|
|
NM_003304.4:c.254G>A
|
NP_003295.1:p.Arg85Lys
|
|
XM_005247738.2:c.34-7025G>A
|
XP_005247795.1:n.34-7025G>A
|
|
XM_005247739.1:c.33+11729G>A
|
XP_005247796.1:n.33+11729G>A
|
|
XR_241506.2:n.782G>A
|
|
|
XR_924164.1:n.782G>A
|
|
|
XR_924165.1:n.782G>A
|
|
|
XR_924166.1:n.782G>A
|
|
|
XM_005247738.4:c.34-7025G>A
|
XP_005247795.1:n.34-7025G>A
|
|
XM_005247739.2:c.33+11729G>A
|
XP_005247796.1:n.33+11729G>A
|
|
XM_017007121.2:c.71G>A
|
XP_016862610.1:p.Arg24Lys
|
|
XR_001740246.1:n.1015G>A
|
|
|
XR_241506.4:n.305G>A
|
|
|
NM_001251845.2:c.254G>A
MANE Select
|
NP_001238774.1:p.Arg85Lys
|
|
NM_003304.5:c.254G>A
|
NP_003295.1:p.Arg85Lys
|
|