ENST00000217958.8:c.*34G>T
MANE Select
|
ENSP00000217958.3:n.*34G>T
|
|
ENST00000217958.7:c.*34G>T
|
ENSP00000217958.3:n.*34G>T
|
|
ENST00000340200.5:c.616G>T
|
ENSP00000345963.5:n.616G>T
|
|
ENST00000361815.9:c.*180G>T
|
ENSP00000354906.5:n.*180G>T
|
|
ENST00000372295.5:c.*34G>T
|
ENSP00000361369.1:n.*34G>T
|
|
ENST00000372296.5:c.*180G>T
|
ENSP00000361370.1:n.*180G>T
|
|
NM_002814.3:c.*34G>T
|
NP_002805.1:n.*34G>T
|
|
NM_170750.2:c.*180G>T
|
NP_736606.1:n.*180G>T
|
|
NM_002814.4:c.*34G>T
MANE Select
|
NP_002805.1:n.*34G>T
|
|
NM_170750.3:c.*180G>T
|
NP_736606.1:n.*180G>T
|
|