ENST00000360124.10:c.1361G>C
|
ENSP00000353241.6:n.1361G>C
|
|
ENST00000645361.2:c.*69G>C
MANE Select
|
ENSP00000496150.1:n.*69G>C
|
|
ENST00000360124.9:c.1181G>C
|
ENSP00000353241.5:n.1181G>C
|
|
ENST00000360608.9:c.*69G>C
|
ENSP00000353820.5:n.*69G>C
|
|
ENST00000389970.7:c.*69G>C
|
ENSP00000374620.4:n.*69G>C
|
|
NM_000106.5:c.*69G>C
|
NP_000097.3:n.*69G>C
|
|
NM_001025161.2:c.*69G>C
|
NP_001020332.2:n.*69G>C
|
|
XM_011529966.1:c.1452+111G>C
|
XP_011528268.1:n.1452+111G>C
|
|
XM_011529967.1:c.1452+111G>C
|
XP_011528269.1:n.1452+111G>C
|
|
XM_011529968.1:c.1452+111G>C
|
XP_011528270.1:n.1452+111G>C
|
|
XM_011529969.1:c.1308+111G>C
|
XP_011528271.1:n.1308+111G>C
|
|
XM_011529970.1:c.1299+111G>C
|
XP_011528272.1:n.1299+111G>C
|
|
XM_011529971.1:c.*69G>C
|
XP_011528273.1:n.*69G>C
|
|
NM_000106.6:c.*69G>C
MANE Select
|
NP_000097.3:n.*69G>C
|
|
NM_001025161.3:c.*69G>C
|
NP_001020332.2:n.*69G>C
|
|