ENST00000360124.10:c.540G>T
|
ENSP00000353241.6:p.Leu180=
|
|
ENST00000645361.2:c.693G>T
MANE Select
|
ENSP00000496150.1:p.Leu231=
|
|
ENST00000359033.4:c.540G>T
|
ENSP00000351927.4:p.Leu180=
|
|
ENST00000360124.9:c.360G>T
|
ENSP00000353241.5:p.Leu120=
|
|
ENST00000360608.9:c.693G>T
|
ENSP00000353820.5:p.Leu231=
|
|
ENST00000389970.7:c.627G>T
|
ENSP00000374620.4:p.Leu209=
|
|
ENST00000488442.1:n.1417G>T
|
|
|
NM_000106.5:c.693G>T
|
NP_000097.3:p.Leu231=
|
|
NM_001025161.2:c.540G>T
|
NP_001020332.2:p.Leu180=
|
|
XM_011529966.1:c.693G>T
|
XP_011528268.1:p.Leu231=
|
|
XM_011529967.1:c.693G>T
|
XP_011528269.1:p.Leu231=
|
|
XM_011529968.1:c.693G>T
|
XP_011528270.1:p.Leu231=
|
|
XM_011529969.1:c.549G>T
|
XP_011528271.1:p.Leu183=
|
|
XM_011529970.1:c.540G>T
|
XP_011528272.1:p.Leu180=
|
|
XM_011529971.1:c.549G>T
|
XP_011528273.1:p.Leu183=
|
|
XM_011529972.1:c.693G>T
|
XP_011528274.1:p.Leu231=
|
|
NM_000106.6:c.693G>T
MANE Select
|
NP_000097.3:p.Leu231=
|
|
NM_001025161.3:c.540G>T
|
NP_001020332.2:p.Leu180=
|
|