ENST00000504915.3:c.7164T>C
|
ENSP00000473355.2:p.Gly2388=
|
|
ENST00000505350.2:c.*7116T>C
|
ENSP00000481752.1:n.*7116T>C
|
|
ENST00000507379.6:c.7056T>C
|
ENSP00000423224.2:p.Gly2352=
|
|
ENST00000509732.6:c.7110T>C
|
ENSP00000426541.2:p.Gly2370=
|
|
ENST00000512211.7:c.7110T>C
|
ENSP00000423828.3:p.Gly2370=
|
|
ENST00000257430.9:c.7110T>C
MANE Select
|
ENSP00000257430.4:p.Gly2370=
|
|
ENST00000257430.8:c.7110T>C
|
ENSP00000257430.4:p.Gly2370=
|
|
ENST00000508376.6:c.7110T>C
|
ENSP00000427089.2:p.Gly2370=
|
|
ENST00000508624.5:c.*6432T>C
|
ENSP00000424265.1:n.*6432T>C
|
|
ENST00000520401.1:c.230+13732T>C
|
|
|
NM_000038.5:c.7110T>C
|
NP_000029.2:p.Gly2370=
|
|
NM_001127510.2:c.7110T>C
|
NP_001120982.1:p.Gly2370=
|
|
NM_001127511.2:c.7056T>C
|
NP_001120983.2:p.Gly2352=
|
|
NM_001354895.1:c.7110T>C
|
NP_001341824.1:p.Gly2370=
|
|
NM_001354896.1:c.7164T>C
|
NP_001341825.1:p.Gly2388=
|
|
NM_001354897.1:c.7140T>C
|
NP_001341826.1:p.Gly2380=
|
|
NM_001354898.1:c.7035T>C
|
NP_001341827.1:p.Gly2345=
|
|
NM_001354899.1:c.7026T>C
|
NP_001341828.1:p.Gly2342=
|
|
NM_001354900.1:c.6987T>C
|
NP_001341829.1:p.Gly2329=
|
|
NM_001354901.1:c.6933T>C
|
NP_001341830.1:p.Gly2311=
|
|
NM_001354902.1:c.6837T>C
|
NP_001341831.1:p.Gly2279=
|
|
NM_001354903.1:c.6807T>C
|
NP_001341832.1:p.Gly2269=
|
|
NM_001354904.1:c.6732T>C
|
NP_001341833.1:p.Gly2244=
|
|
NM_001354905.1:c.6630T>C
|
NP_001341834.1:p.Gly2210=
|
|
NM_001354906.1:c.6261T>C
|
NP_001341835.1:p.Gly2087=
|
|
NM_000038.6:c.7110T>C
MANE Select
|
NP_000029.2:p.Gly2370=
|
|
NM_001127510.3:c.7110T>C
|
NP_001120982.1:p.Gly2370=
|
|
NM_001127511.3:c.7056T>C
|
NP_001120983.2:p.Gly2352=
|
|
NM_001354895.2:c.7110T>C
|
NP_001341824.1:p.Gly2370=
|
|
NM_001354896.2:c.7164T>C
|
NP_001341825.1:p.Gly2388=
|
|
NM_001354897.2:c.7140T>C
|
NP_001341826.1:p.Gly2380=
|
|
NM_001354898.2:c.7035T>C
|
NP_001341827.1:p.Gly2345=
|
|
NM_001354899.2:c.7026T>C
|
NP_001341828.1:p.Gly2342=
|
|
NM_001354900.2:c.6987T>C
|
NP_001341829.1:p.Gly2329=
|
|
NM_001354901.2:c.6933T>C
|
NP_001341830.1:p.Gly2311=
|
|
NM_001354902.2:c.6837T>C
|
NP_001341831.1:p.Gly2279=
|
|
NM_001354903.2:c.6807T>C
|
NP_001341832.1:p.Gly2269=
|
|
NM_001354904.2:c.6732T>C
|
NP_001341833.1:p.Gly2244=
|
|
NM_001354905.2:c.6630T>C
|
NP_001341834.1:p.Gly2210=
|
|
NM_001354906.2:c.6261T>C
|
NP_001341835.1:p.Gly2087=
|
|