ENST00000682153.1:c.6122-353C>T
|
ENSP00000507923.1:n.6122-353C>T
|
|
ENST00000682358.1:n.6192-353C>T
|
|
|
ENST00000683334.1:c.*1804-353C>T
|
ENSP00000507369.1:n.*1804-353C>T
|
|
ENST00000357162.7:c.6047-353C>T
MANE Select
|
ENSP00000349685.2:n.6047-353C>T
|
|
ENST00000358544.7:c.6122-353C>T
MANE Plus Clinical
|
ENSP00000351346.2:n.6122-353C>T
|
|
ENST00000357162.6:c.6047-353C>T
|
ENSP00000349685.2:n.6047-353C>T
|
|
ENST00000358544.6:c.6122-353C>T
|
ENSP00000351346.2:n.6122-353C>T
|
|
NM_017890.4:c.6122-353C>T , LRG_351t1:c.6122-353C>T
|
NP_060360.3:n.6122-353C>T
|
|
NM_152564.4:c.6047-353C>T , LRG_351t2:c.6047-353C>T
|
NP_689777.3:n.6047-353C>T
|
|
XM_005250800.2:c.6122-353C>T
|
XP_005250857.1:n.6122-353C>T
|
|
XM_005250801.3:c.6122-353C>T
|
XP_005250858.1:n.6122-353C>T
|
|
XM_011516848.1:c.6119-353C>T
|
XP_011515150.1:n.6119-353C>T
|
|
XM_011516849.1:c.6044-353C>T
|
XP_011515151.1:n.6044-353C>T
|
|
XM_011516850.1:c.5744-353C>T
|
XP_011515152.1:n.5744-353C>T
|
|
XM_011516851.1:c.3008-353C>T
|
XP_011515153.1:n.3008-353C>T
|
|
XM_011516852.1:c.3008-353C>T
|
XP_011515154.1:n.3008-353C>T
|
|
XM_011516853.1:c.6122-353C>T
|
XP_011515155.1:n.6122-353C>T
|
|
XM_011516854.1:c.1901-353C>T
|
XP_011515156.1:n.1901-353C>T
|
|
XM_005250800.3:c.6122-353C>T
|
XP_005250857.1:n.6122-353C>T
|
|
XM_005250801.5:c.6122-353C>T
|
XP_005250858.1:n.6122-353C>T
|
|
XM_011516848.2:c.6119-353C>T
|
XP_011515150.1:n.6119-353C>T
|
|
XM_011516849.2:c.6044-353C>T
|
XP_011515151.1:n.6044-353C>T
|
|
XM_011516850.2:c.5744-353C>T
|
XP_011515152.1:n.5744-353C>T
|
|
XM_011516851.2:c.3008-353C>T
|
XP_011515153.1:n.3008-353C>T
|
|
XM_011516852.2:c.3008-353C>T
|
XP_011515154.1:n.3008-353C>T
|
|
XM_011516853.2:c.6122-353C>T
|
XP_011515155.1:n.6122-353C>T
|
|
XM_011516854.2:c.1901-353C>T
|
XP_011515156.1:n.1901-353C>T
|
|
XM_017013109.1:c.5927-353C>T
|
XP_016868598.1:n.5927-353C>T
|
|
XM_017013111.1:c.3008-353C>T
|
XP_016868600.1:n.3008-353C>T
|
|
XM_017013112.1:c.1679-353C>T
|
XP_016868601.1:n.1679-353C>T
|
|
XM_024447074.1:c.4907-353C>T
|
XP_024302842.1:n.4907-353C>T
|
|
XR_001745482.2:n.6083-353C>T
|
|
|
NM_017890.5:c.6122-353C>T
MANE Plus Clinical
|
NP_060360.3:n.6122-353C>T
|
|
NM_152564.5:c.6047-353C>T
MANE Select
|
NP_689777.3:n.6047-353C>T
|
|