ENST00000360124.10:c.1313G>T
|
ENSP00000353241.6:n.1313G>T
|
|
ENST00000645361.2:c.*21G>T
MANE Select
|
ENSP00000496150.1:n.*21G>T
|
|
ENST00000360124.9:c.1133G>T
|
ENSP00000353241.5:n.1133G>T
|
|
ENST00000360608.9:c.*21G>T
|
ENSP00000353820.5:n.*21G>T
|
|
ENST00000389970.7:c.*21G>T
|
ENSP00000374620.4:n.*21G>T
|
|
ENST00000488442.1:n.2239G>T
|
|
|
NM_000106.5:c.*21G>T
|
NP_000097.3:n.*21G>T
|
|
NM_001025161.2:c.*21G>T
|
NP_001020332.2:n.*21G>T
|
|
XM_011529966.1:c.1452+63G>T
|
XP_011528268.1:n.1452+63G>T
|
|
XM_011529967.1:c.1452+63G>T
|
XP_011528269.1:n.1452+63G>T
|
|
XM_011529968.1:c.1452+63G>T
|
XP_011528270.1:n.1452+63G>T
|
|
XM_011529969.1:c.1308+63G>T
|
XP_011528271.1:n.1308+63G>T
|
|
XM_011529970.1:c.1299+63G>T
|
XP_011528272.1:n.1299+63G>T
|
|
XM_011529971.1:c.*21G>T
|
XP_011528273.1:n.*21G>T
|
|
NM_000106.6:c.*21G>T
MANE Select
|
NP_000097.3:n.*21G>T
|
|
NM_001025161.3:c.*21G>T
|
NP_001020332.2:n.*21G>T
|
|