ENST00000360124.10:c.827G>T
|
ENSP00000353241.6:n.827G>T
|
|
ENST00000645361.2:c.1029G>T
MANE Select
|
ENSP00000496150.1:p.Arg343=
|
|
ENST00000359033.4:c.876G>T
|
ENSP00000351927.4:p.Arg292=
|
|
ENST00000360124.9:c.647G>T
|
ENSP00000353241.5:n.647G>T
|
|
ENST00000360608.9:c.1029G>T
|
ENSP00000353820.5:p.Arg343=
|
|
ENST00000389970.7:c.1020G>T
|
ENSP00000374620.4:p.Arg340=
|
|
ENST00000488442.1:n.1753G>T
|
|
|
NM_000106.5:c.1029G>T
|
NP_000097.3:p.Arg343=
|
|
NM_001025161.2:c.876G>T
|
NP_001020332.2:p.Arg292=
|
|
XM_011529966.1:c.1029G>T
|
XP_011528268.1:p.Arg343=
|
|
XM_011529967.1:c.1029G>T
|
XP_011528269.1:p.Arg343=
|
|
XM_011529968.1:c.1029G>T
|
XP_011528270.1:p.Arg343=
|
|
XM_011529969.1:c.885G>T
|
XP_011528271.1:p.Arg295=
|
|
XM_011529970.1:c.876G>T
|
XP_011528272.1:p.Arg292=
|
|
XM_011529971.1:c.885G>T
|
XP_011528273.1:p.Arg295=
|
|
XM_011529972.1:c.*14G>T
|
XP_011528274.1:n.*14G>T
|
|
NM_000106.6:c.1029G>T
MANE Select
|
NP_000097.3:p.Arg343=
|
|
NM_001025161.3:c.876G>T
|
NP_001020332.2:p.Arg292=
|
|