ENST00000578493.2:n.834G>C
|
|
|
ENST00000699291.1:c.626G>C
|
ENSP00000514272.1:n.626G>C
|
|
ENST00000699292.1:n.541G>C
|
|
|
ENST00000225275.4:c.1501G>C
MANE Select
|
ENSP00000225275.3:p.Gly501Arg
|
|
ENST00000225275.3:c.1501G>C
|
ENSP00000225275.3:p.Gly501Arg
|
|
NM_000250.1:c.1501G>C , LRG_84t1:c.1501G>C
|
NP_000241.1:p.Gly501Arg
|
|
XM_011524821.1:c.1687G>C
|
XP_011523123.1:p.Gly563Arg
|
|
XM_011524822.1:c.1216G>C
|
XP_011523124.1:p.Gly406Arg
|
|
XM_011524823.1:c.*50G>C
|
XP_011523125.1:n.*50G>C
|
|
NM_000250.2:c.1501G>C
MANE Select
|
NP_000241.1:p.Gly501Arg
|
|