ENST00000405094.2:c.*732G>T
MANE Select
|
ENSP00000385823.1:n.*732G>T
|
|
ENST00000405592.5:c.*732G>T
|
ENSP00000383973.1:n.*732G>T
|
|
ENST00000406652.5:c.*732G>T
|
ENSP00000384249.1:n.*732G>T
|
|
NM_001282755.1:c.*732G>T
|
NP_001269684.1:n.*732G>T
|
|
NM_001282756.1:c.*732G>T
|
NP_001269685.1:n.*732G>T
|
|
XM_005264456.2:c.*732G>T
|
XP_005264513.1:n.*732G>T
|
|
XM_005264458.2:c.*732G>T
|
XP_005264515.1:n.*732G>T
|
|
XM_005264459.2:c.*732G>T
|
XP_005264516.1:n.*732G>T
|
|
XM_011533006.1:c.*732G>T
|
XP_011531308.1:n.*732G>T
|
|
XR_939697.1:n.1791-29784G>T
|
|
|
XR_939698.1:n.2548G>T
|
|
|
NM_001330442.1:c.*732G>T
|
NP_001317371.1:n.*732G>T
|
|
NM_001330443.1:c.*732G>T
|
NP_001317372.1:n.*732G>T
|
|
NM_001330444.1:c.*732G>T
|
NP_001317373.1:n.*732G>T
|
|
XM_024453019.1:c.*732G>T
|
XP_024308787.1:n.*732G>T
|
|
XR_001738859.2:n.1794-29784G>T
|
|
|
XR_001738860.2:n.2548G>T
|
|
|
XR_939697.3:n.1794-29784G>T
|
|
|
NM_001330442.2:c.*732G>T
MANE Select
|
NP_001317371.1:n.*732G>T
|
|
NM_001330443.2:c.*732G>T
|
NP_001317372.1:n.*732G>T
|
|
NM_001330444.2:c.*732G>T
|
NP_001317373.1:n.*732G>T
|
|
NM_001282755.2:c.*732G>T
|
NP_001269684.1:n.*732G>T
|
|
NM_001282756.2:c.*732G>T
|
NP_001269685.1:n.*732G>T
|
|