ENST00000695527.1:n.20A>T
|
|
|
ENST00000695558.1:c.5708A>T
|
ENSP00000512015.1:p.Glu1903Val
|
|
ENST00000703224.1:c.*4918A>T
|
ENSP00000515242.1:n.*4918A>T
|
|
ENST00000359568.10:c.5675A>T
MANE Select
|
ENSP00000352572.5:p.Glu1892Val
|
|
ENST00000359568.9:c.5675A>T
|
ENSP00000352572.5:p.Glu1892Val
|
|
ENST00000480896.5:n.5944A>T
|
|
|
NM_001315529.1:c.5321A>T
|
NP_001302458.1:p.Glu1774Val
|
|
NM_006031.5:c.5675A>T
|
NP_006022.3:p.Glu1892Val
|
|
XM_005261124.3:c.5708A>T
|
XP_005261181.1:p.Glu1903Val
|
|
XM_011529593.1:c.5786A>T
|
XP_011527895.1:p.Glu1929Val
|
|
XM_011529594.1:c.5756A>T
|
XP_011527896.1:p.Glu1919Val
|
|
XM_005261124.5:c.5708A>T
|
XP_005261181.1:p.Glu1903Val
|
|
XM_011529594.3:c.5756A>T
|
XP_011527896.1:p.Glu1919Val
|
|
XM_017028362.2:c.5675A>T
|
XP_016883851.1:p.Glu1892Val
|
|
XM_017028363.1:c.5354A>T
|
XP_016883852.1:p.Glu1785Val
|
|
XM_024452082.1:c.4592A>T
|
XP_024307850.1:p.Glu1531Val
|
|
XM_024452083.1:c.3488A>T
|
XP_024307851.1:p.Glu1163Val
|
|
NM_006031.6:c.5675A>T
MANE Select
|
NP_006022.3:p.Glu1892Val
|
|
NM_001315529.2:c.5321A>T
|
NP_001302458.1:p.Glu1774Val
|
|