ENST00000360124.10:c.691-14G=
|
ENSP00000353241.6:n.691-14G=
|
|
ENST00000645361.2:c.879G=
MANE Select
|
ENSP00000496150.1:p.Glu293=
|
|
ENST00000359033.4:c.726G=
|
ENSP00000351927.4:p.Glu242=
|
|
ENST00000360124.9:c.511-14G=
|
ENSP00000353241.5:n.511-14G=
|
|
ENST00000360608.9:c.879G=
|
ENSP00000353820.5:p.Glu293=
|
|
ENST00000389970.7:c.813G=
|
ENSP00000374620.4:p.Glu271=
|
|
ENST00000488442.1:n.1603G=
|
|
|
NM_000106.5:c.879G=
|
NP_000097.3:p.Glu293=
|
|
NM_001025161.2:c.726G=
|
NP_001020332.2:p.Glu242=
|
|
XM_011529966.1:c.879G=
|
XP_011528268.1:p.Glu293=
|
|
XM_011529967.1:c.879G=
|
XP_011528269.1:p.Glu293=
|
|
XM_011529968.1:c.879G=
|
XP_011528270.1:p.Glu293=
|
|
XM_011529969.1:c.735G=
|
XP_011528271.1:p.Glu245=
|
|
XM_011529970.1:c.726G=
|
XP_011528272.1:p.Glu242=
|
|
XM_011529971.1:c.735G=
|
XP_011528273.1:p.Glu245=
|
|
XM_011529972.1:c.843+226G=
|
XP_011528274.1:n.843+226G=
|
|
NM_000106.6:c.879G=
MANE Select
|
NP_000097.3:p.Glu293=
|
|
NM_001025161.3:c.726G=
|
NP_001020332.2:p.Glu242=
|
|