|
NM_015291.4:c.338G>A
MANE Select
|
NP_056106.1:p.Arg113His
|
|
ENST00000375847.8:c.338G>A
MANE Select
|
ENSP00000365007.3:p.Arg113His
|
|
NM_001287811.1:c.-599G>A
|
NP_001274740.1:n.-599G>A
|
|
NM_001287811.2:c.-599G>A
|
NP_001274740.1:n.-599G>A
|
|
NM_015291.3:c.338G>A
|
NP_056106.1:p.Arg113His
|
|
NR_109898.1:n.502G>A
|
|
|
NR_109898.2:n.467G>A
|
|
|
ENST00000375838.5:c.338G>A
|
ENSP00000364998.1:p.Arg113His
|
|
ENST00000375847.7:c.338G>A
|
ENSP00000365007.3:p.Arg113His
|
|
ENST00000375849.5:c.338G>A
|
ENSP00000365009.1:p.Arg113His
|
|
ENST00000475133.5:c.338G>A
|
ENSP00000431886.1:p.Arg113His
|
|
ENST00000616884.4:c.-599G>A
|
ENSP00000480224.1:n.-599G>A
|
|
XR_001737078.1:n.621G>A
|
|
|
XR_001737079.2:n.621G>A
|
|