ENST00000435063.4:n.1597G>T
|
|
|
ENST00000354724.8:c.*871G>T
MANE Select
|
ENSP00000346761.3:n.*871G>T
|
|
ENST00000435063.3:n.1586G>T
|
|
|
ENST00000519075.2:n.3394G>T
|
|
|
ENST00000521111.2:n.3098G>T
|
|
|
ENST00000523531.2:n.2036G>T
|
|
|
ENST00000523976.2:c.*871G>T
|
ENSP00000429792.1:n.*871G>T
|
|
ENST00000674160.1:c.*1526G>T
|
ENSP00000501529.1:n.*1526G>T
|
|
ENST00000674177.1:c.*1613G>T
|
ENSP00000501471.1:n.*1613G>T
|
|
ENST00000674295.1:c.*871G>T
|
ENSP00000501320.1:n.*871G>T
|
|
ENST00000674358.1:c.*871G>T
|
ENSP00000501370.1:n.*871G>T
|
|
ENST00000674418.1:c.*871G>T
|
ENSP00000501342.1:n.*871G>T
|
|
ENST00000674439.1:n.2014G>T
|
|
|
ENST00000337919.9:c.*871G>T
|
ENSP00000338272.5:n.*871G>T
|
|
ENST00000354724.7:c.*871G>T
|
ENSP00000346761.3:n.*871G>T
|
|
NM_001040708.1:c.*871G>T
|
NP_001035798.1:n.*871G>T
|
|
NM_001282851.1:c.*871G>T
|
NP_001269780.1:n.*871G>T
|
|
NM_012258.3:c.*871G>T
|
NP_036390.3:n.*871G>T
|
|
NM_012258.4:c.*871G>T
MANE Select
|
NP_036390.3:n.*871G>T
|
|
NM_001040708.2:c.*871G>T
|
NP_001035798.1:n.*871G>T
|
|
NM_001282851.2:c.*871G>T
|
NP_001269780.1:n.*871G>T
|
|