ENST00000682153.1:c.8704T>C
|
ENSP00000507923.1:p.Tyr2902His
|
|
ENST00000682358.1:n.8774T>C
|
|
|
ENST00000683334.1:c.*4386T>C
|
ENSP00000507369.1:n.*4386T>C
|
|
ENST00000357162.7:c.8629T>C
MANE Select
|
ENSP00000349685.2:p.Tyr2877His
|
|
ENST00000358544.7:c.8704T>C
MANE Plus Clinical
|
ENSP00000351346.2:p.Tyr2902His
|
|
ENST00000357162.6:c.8629T>C
|
ENSP00000349685.2:p.Tyr2877His
|
|
ENST00000358544.6:c.8704T>C
|
ENSP00000351346.2:p.Tyr2902His
|
|
NM_017890.4:c.8704T>C , LRG_351t1:c.8704T>C
|
NP_060360.3:p.Tyr2902His
|
|
NM_152564.4:c.8629T>C , LRG_351t2:c.8629T>C
|
NP_689777.3:p.Tyr2877His
|
|
XM_005250800.2:c.8704T>C
|
XP_005250857.1:p.Tyr2902His
|
|
XM_005250801.3:c.8704T>C
|
XP_005250858.1:p.Tyr2902His
|
|
XM_011516848.1:c.8701T>C
|
XP_011515150.1:p.Tyr2901His
|
|
XM_011516849.1:c.8626T>C
|
XP_011515151.1:p.Tyr2876His
|
|
XM_011516850.1:c.8326T>C
|
XP_011515152.1:p.Tyr2776His
|
|
XM_011516851.1:c.5590T>C
|
XP_011515153.1:p.Tyr1864His
|
|
XM_011516852.1:c.5590T>C
|
XP_011515154.1:p.Tyr1864His
|
|
XM_011516854.1:c.4483T>C
|
XP_011515156.1:p.Tyr1495His
|
|
XM_005250800.3:c.8704T>C
|
XP_005250857.1:p.Tyr2902His
|
|
XM_005250801.5:c.8704T>C
|
XP_005250858.1:p.Tyr2902His
|
|
XM_011516848.2:c.8701T>C
|
XP_011515150.1:p.Tyr2901His
|
|
XM_011516849.2:c.8626T>C
|
XP_011515151.1:p.Tyr2876His
|
|
XM_011516850.2:c.8326T>C
|
XP_011515152.1:p.Tyr2776His
|
|
XM_011516851.2:c.5590T>C
|
XP_011515153.1:p.Tyr1864His
|
|
XM_011516852.2:c.5590T>C
|
XP_011515154.1:p.Tyr1864His
|
|
XM_011516854.2:c.4483T>C
|
XP_011515156.1:p.Tyr1495His
|
|
XM_017013109.1:c.8509T>C
|
XP_016868598.1:p.Tyr2837His
|
|
XM_017013111.1:c.5590T>C
|
XP_016868600.1:p.Tyr1864His
|
|
XM_017013112.1:c.4261T>C
|
XP_016868601.1:p.Tyr1421His
|
|
XM_024447074.1:c.7489T>C
|
XP_024302842.1:p.Tyr2497His
|
|
NM_017890.5:c.8704T>C
MANE Plus Clinical
|
NP_060360.3:p.Tyr2902His
|
|
NM_152564.5:c.8629T>C
MANE Select
|
NP_689777.3:p.Tyr2877His
|
|