ENST00000360124.10:c.1115C>A
|
ENSP00000353241.6:n.1115C>A
|
|
ENST00000645361.2:c.1317C>A
MANE Select
|
ENSP00000496150.1:p.Gly439=
|
|
ENST00000359033.4:c.1164C>A
|
ENSP00000351927.4:p.Gly388=
|
|
ENST00000360124.9:c.935C>A
|
ENSP00000353241.5:n.935C>A
|
|
ENST00000360608.9:c.1317C>A
|
ENSP00000353820.5:p.Gly439=
|
|
ENST00000389970.7:c.1308C>A
|
ENSP00000374620.4:p.Gly436=
|
|
ENST00000488442.1:n.2041C>A
|
|
|
NM_000106.5:c.1317C>A
|
NP_000097.3:p.Gly439=
|
|
NM_001025161.2:c.1164C>A
|
NP_001020332.2:p.Gly388=
|
|
XM_011529966.1:c.1317C>A
|
XP_011528268.1:p.Gly439=
|
|
XM_011529967.1:c.1317C>A
|
XP_011528269.1:p.Gly439=
|
|
XM_011529968.1:c.1317C>A
|
XP_011528270.1:p.Gly439=
|
|
XM_011529969.1:c.1173C>A
|
XP_011528271.1:p.Gly391=
|
|
XM_011529970.1:c.1164C>A
|
XP_011528272.1:p.Gly388=
|
|
XM_011529971.1:c.1173C>A
|
XP_011528273.1:p.Gly391=
|
|
NM_000106.6:c.1317C>A
MANE Select
|
NP_000097.3:p.Gly439=
|
|
NM_001025161.3:c.1164C>A
|
NP_001020332.2:p.Gly388=
|
|