ENST00000360124.10:c.618G>C
|
ENSP00000353241.6:p.Glu206Asp
|
|
ENST00000645361.2:c.771G>C
MANE Select
|
ENSP00000496150.1:p.Glu257Asp
|
|
ENST00000359033.4:c.618G>C
|
ENSP00000351927.4:p.Glu206Asp
|
|
ENST00000360124.9:c.438G>C
|
ENSP00000353241.5:p.Glu146Asp
|
|
ENST00000360608.9:c.771G>C
|
ENSP00000353820.5:p.Glu257Asp
|
|
ENST00000389970.7:c.705G>C
|
ENSP00000374620.4:p.Glu235Asp
|
|
ENST00000488442.1:n.1495G>C
|
|
|
NM_000106.5:c.771G>C
|
NP_000097.3:p.Glu257Asp
|
|
NM_001025161.2:c.618G>C
|
NP_001020332.2:p.Glu206Asp
|
|
XM_011529966.1:c.771G>C
|
XP_011528268.1:p.Glu257Asp
|
|
XM_011529967.1:c.771G>C
|
XP_011528269.1:p.Glu257Asp
|
|
XM_011529968.1:c.771G>C
|
XP_011528270.1:p.Glu257Asp
|
|
XM_011529969.1:c.627G>C
|
XP_011528271.1:p.Glu209Asp
|
|
XM_011529970.1:c.618G>C
|
XP_011528272.1:p.Glu206Asp
|
|
XM_011529971.1:c.627G>C
|
XP_011528273.1:p.Glu209Asp
|
|
XM_011529972.1:c.771G>C
|
XP_011528274.1:p.Glu257Asp
|
|
NM_000106.6:c.771G>C
MANE Select
|
NP_000097.3:p.Glu257Asp
|
|
NM_001025161.3:c.618G>C
|
NP_001020332.2:p.Glu206Asp
|
|