ENST00000682153.1:c.*475T>C
|
ENSP00000507923.1:n.*475T>C
|
|
ENST00000682358.1:n.11451T>C
|
|
|
ENST00000683334.1:c.*7063T>C
|
ENSP00000507369.1:n.*7063T>C
|
|
ENST00000357162.7:c.11306T>C
MANE Select
|
ENSP00000349685.2:p.Val3769Ala
|
|
ENST00000358544.7:c.11381T>C
MANE Plus Clinical
|
ENSP00000351346.2:p.Val3794Ala
|
|
ENST00000357162.6:c.11306T>C
|
ENSP00000349685.2:p.Val3769Ala
|
|
ENST00000358544.6:c.11381T>C
|
ENSP00000351346.2:p.Val3794Ala
|
|
ENST00000493587.1:n.323T>C
|
|
|
NM_017890.4:c.11381T>C , LRG_351t1:c.11381T>C
|
NP_060360.3:p.Val3794Ala
|
|
NM_152564.4:c.11306T>C , LRG_351t2:c.11306T>C
|
NP_689777.3:p.Val3769Ala
|
|
XM_005250800.2:c.11381T>C
|
XP_005250857.1:p.Val3794Ala
|
|
XM_005250801.3:c.11381T>C
|
XP_005250858.1:p.Val3794Ala
|
|
XM_011516848.1:c.11378T>C
|
XP_011515150.1:p.Val3793Ala
|
|
XM_011516849.1:c.11303T>C
|
XP_011515151.1:p.Val3768Ala
|
|
XM_011516850.1:c.11003T>C
|
XP_011515152.1:p.Val3668Ala
|
|
XM_011516851.1:c.8267T>C
|
XP_011515153.1:p.Val2756Ala
|
|
XM_011516852.1:c.8267T>C
|
XP_011515154.1:p.Val2756Ala
|
|
XM_011516854.1:c.7160T>C
|
XP_011515156.1:p.Val2387Ala
|
|
XM_005250800.3:c.11381T>C
|
XP_005250857.1:p.Val3794Ala
|
|
XM_005250801.5:c.11381T>C
|
XP_005250858.1:p.Val3794Ala
|
|
XM_011516848.2:c.11378T>C
|
XP_011515150.1:p.Val3793Ala
|
|
XM_011516849.2:c.11303T>C
|
XP_011515151.1:p.Val3768Ala
|
|
XM_011516850.2:c.11003T>C
|
XP_011515152.1:p.Val3668Ala
|
|
XM_011516851.2:c.8267T>C
|
XP_011515153.1:p.Val2756Ala
|
|
XM_011516852.2:c.8267T>C
|
XP_011515154.1:p.Val2756Ala
|
|
XM_011516854.2:c.7160T>C
|
XP_011515156.1:p.Val2387Ala
|
|
XM_017013109.1:c.11186T>C
|
XP_016868598.1:p.Val3729Ala
|
|
XM_017013111.1:c.8267T>C
|
XP_016868600.1:p.Val2756Ala
|
|
XM_017013112.1:c.6938T>C
|
XP_016868601.1:p.Val2313Ala
|
|
XM_024447074.1:c.10166T>C
|
XP_024302842.1:p.Val3389Ala
|
|
NM_017890.5:c.11381T>C
MANE Plus Clinical
|
NP_060360.3:p.Val3794Ala
|
|
NM_152564.5:c.11306T>C
MANE Select
|
NP_689777.3:p.Val3769Ala
|
|