ENST00000682153.1:c.7262T>G
|
ENSP00000507923.1:p.Val2421Gly
|
|
ENST00000682358.1:n.7332T>G
|
|
|
ENST00000683334.1:c.*2944T>G
|
ENSP00000507369.1:n.*2944T>G
|
|
ENST00000357162.7:c.7187T>G
MANE Select
|
ENSP00000349685.2:p.Val2396Gly
|
|
ENST00000358544.7:c.7262T>G
MANE Plus Clinical
|
ENSP00000351346.2:p.Val2421Gly
|
|
ENST00000357162.6:c.7187T>G
|
ENSP00000349685.2:p.Val2396Gly
|
|
ENST00000358544.6:c.7262T>G
|
ENSP00000351346.2:p.Val2421Gly
|
|
ENST00000518569.1:n.317T>G
|
|
|
NM_017890.4:c.7262T>G , LRG_351t1:c.7262T>G
|
NP_060360.3:p.Val2421Gly
|
|
NM_152564.4:c.7187T>G , LRG_351t2:c.7187T>G
|
NP_689777.3:p.Val2396Gly
|
|
XM_005250800.2:c.7262T>G
|
XP_005250857.1:p.Val2421Gly
|
|
XM_005250801.3:c.7262T>G
|
XP_005250858.1:p.Val2421Gly
|
|
XM_011516848.1:c.7259T>G
|
XP_011515150.1:p.Val2420Gly
|
|
XM_011516849.1:c.7184T>G
|
XP_011515151.1:p.Val2395Gly
|
|
XM_011516850.1:c.6884T>G
|
XP_011515152.1:p.Val2295Gly
|
|
XM_011516851.1:c.4148T>G
|
XP_011515153.1:p.Val1383Gly
|
|
XM_011516852.1:c.4148T>G
|
XP_011515154.1:p.Val1383Gly
|
|
XM_011516853.1:c.7262T>G
|
XP_011515155.1:p.Val2421Gly
|
|
XM_011516854.1:c.3041T>G
|
XP_011515156.1:p.Val1014Gly
|
|
XR_928446.1:n.2065+3778A>C
|
|
|
XM_005250800.3:c.7262T>G
|
XP_005250857.1:p.Val2421Gly
|
|
XM_005250801.5:c.7262T>G
|
XP_005250858.1:p.Val2421Gly
|
|
XM_011516848.2:c.7259T>G
|
XP_011515150.1:p.Val2420Gly
|
|
XM_011516849.2:c.7184T>G
|
XP_011515151.1:p.Val2395Gly
|
|
XM_011516850.2:c.6884T>G
|
XP_011515152.1:p.Val2295Gly
|
|
XM_011516851.2:c.4148T>G
|
XP_011515153.1:p.Val1383Gly
|
|
XM_011516852.2:c.4148T>G
|
XP_011515154.1:p.Val1383Gly
|
|
XM_011516853.2:c.7262T>G
|
XP_011515155.1:p.Val2421Gly
|
|
XM_011516854.2:c.3041T>G
|
XP_011515156.1:p.Val1014Gly
|
|
XM_017013109.1:c.7067T>G
|
XP_016868598.1:p.Val2356Gly
|
|
XM_017013111.1:c.4148T>G
|
XP_016868600.1:p.Val1383Gly
|
|
XM_017013112.1:c.2819T>G
|
XP_016868601.1:p.Val940Gly
|
|
XM_024447074.1:c.6047T>G
|
XP_024302842.1:p.Val2016Gly
|
|
NM_017890.5:c.7262T>G
MANE Plus Clinical
|
NP_060360.3:p.Val2421Gly
|
|
NM_152564.5:c.7187T>G
MANE Select
|
NP_689777.3:p.Val2396Gly
|
|