|
NM_018196.4:c.278G>A
MANE Select
|
NP_060666.1:p.Arg93His
|
|
ENST00000334398.8:c.278G>A
MANE Select
|
ENSP00000335261.3:p.Arg93His
|
|
NM_001184797.1:c.278G>A
|
NP_001171726.1:p.Arg93His
|
|
NM_001184797.2:c.278G>A
|
NP_001171726.1:p.Arg93His
|
|
NM_018196.3:c.278G>A
|
NP_060666.1:p.Arg93His
|
|
ENST00000334398.7:c.278G>A
|
ENSP00000335261.3:p.Arg93His
|
|
ENST00000369439.4:c.278G>A
|
ENSP00000358447.4:p.Arg93His
|
|
ENST00000487422.1:n.279G>A
|
|
|
ENST00000675642.1:c.311G>A
|
ENSP00000502604.1:p.Arg104His
|
|
XM_011531182.1:c.125G>A
|
XP_011529484.1:p.Arg42His
|
|
XM_011531182.3:c.125G>A
|
XP_011529484.1:p.Arg42His
|
|
XM_017029620.2:c.278G>A
|
XP_016885109.1:p.Arg93His
|
|
XR_247318.1:n.449G>A
|
|
|
XR_247318.3:n.423G>A
|
|