|
ENST00000395796.8:c.*1396A>C
|
ENSP00000379142.4:n.*1396A>C
|
|
|
ENST00000616242.5:c.*518A>C
|
ENSP00000482149.2:n.*518A>C
|
|
|
ENST00000683378.1:n.624A>C
|
|
|
|
ENST00000336642.9:c.432A>C
|
ENSP00000338009.5:p.Ter144Cys
|
|
|
ENST00000345378.7:c.1401A>C
|
ENSP00000223366.2:p.Ter467Cys
|
|
|
ENST00000403799.8:c.1398A>C
MANE Select
|
ENSP00000384247.3:p.Ter466Cys
|
|
|
ENST00000671824.1:c.1461A>C
|
ENSP00000500264.1:p.Ter487Cys
|
|
|
ENST00000672743.1:n.381+29A>C
|
|
|
|
ENST00000673284.1:c.1369+29A>C
|
ENSP00000499852.1:n.1369+29A>C
|
|
|
ENST00000336642.8:c.450A>C
|
ENSP00000338009.4:p.Ter150Cys
|
|
|
ENST00000345378.6:c.1401A>C
|
ENSP00000223366.2:p.Ter467Cys
|
|
|
ENST00000395796.7:c.1395A>C
|
ENSP00000379142.3:p.Ter465Cys
|
|
|
ENST00000403799.7:c.1398A>C
|
ENSP00000384247.3:p.Ter466Cys
|
|
|
ENST00000437084.1:c.1347A>C
|
ENSP00000402840.1:p.Ter449Cys
|
|
|
ENST00000459642.1:n.778A>C
|
|
|
|
ENST00000616242.4:c.1395A>C
|
ENSP00000482149.1:p.Ter465Cys
|
|
|
NM_000162.3:c.1398A>C
|
NP_000153.1:p.Ter466Cys
|
|
|
NM_033507.1:c.1401A>C
|
NP_277042.1:p.Ter467Cys
|
|
|
NM_033508.1:c.1395A>C
|
NP_277043.1:p.Ter465Cys
|
|
|
NM_000162.4:c.1398A>C
|
NP_000153.1:p.Ter466Cys
|
|
|
NM_001354800.1:c.1369+29A>C
|
NP_001341729.1:n.1369+29A>C
|
|
|
NM_001354801.1:c.387A>C
|
NP_001341730.1:p.Ter129Cys
|
|
|
NM_001354802.1:c.229+29A>C
|
NP_001341731.1:n.229+29A>C
|
|
|
NM_001354803.1:c.432A>C
|
NP_001341732.1:p.Ter144Cys
|
|
|
NM_033507.2:c.1401A>C
|
NP_277042.1:p.Ter467Cys
|
|
|
NM_033508.2:c.1395A>C
|
NP_277043.1:p.Ter465Cys
|
|
|
XM_024446707.1:c.258A>C
|
XP_024302475.1:p.Ter86Cys
|
|
|
NM_000162.5:c.1398A>C
MANE Select
|
NP_000153.1:p.Ter466Cys
|
|
|
NM_033507.3:c.1401A>C
|
NP_277042.1:p.Ter467Cys
|
|
|
NM_033508.3:c.1395A>C
|
NP_277043.1:p.Ter465Cys
|
|
|
NM_001354803.2:c.432A>C
|
NP_001341732.1:p.Ter144Cys
|
|
