|
ENST00000696964.1:c.1537T>G
|
ENSP00000513003.1:p.Leu513Val
|
|
|
ENST00000269197.12:c.1534T>G
MANE Select
|
ENSP00000269197.4:p.Leu512Val
|
|
|
ENST00000592288.6:c.*658T>G
|
ENSP00000465053.1:n.*658T>G
|
|
|
ENST00000592541.6:c.*1193T>G
|
ENSP00000466655.2:n.*1193T>G
|
|
|
ENST00000593195.6:c.1746T>G
|
ENSP00000466073.1:n.1746T>G
|
|
|
ENST00000642541.1:c.1366T>G
|
ENSP00000493665.1:p.Leu456Val
|
|
|
ENST00000681521.1:c.1414T>G
|
ENSP00000506037.1:p.Leu472Val
|
|
|
ENST00000269197.9:c.1534T>G
|
ENSP00000269197.4:p.Leu512Val
|
|
|
ENST00000592288.5:c.*658T>G
|
ENSP00000465053.1:n.*658T>G
|
|
|
NM_030632.1:c.1534T>G
|
NP_085135.1:p.Leu512Val
|
|
|
XM_005258356.1:c.1537T>G
|
XP_005258413.1:p.Leu513Val
|
|
|
XM_011526205.1:c.1510T>G
|
XP_011524507.1:p.Leu504Val
|
|
|
XM_011526206.1:c.1456T>G
|
XP_011524508.1:p.Leu486Val
|
|
|
XM_011526207.1:c.1456T>G
|
XP_011524509.1:p.Leu486Val
|
|
|
XM_011526208.1:c.1417T>G
|
XP_011524510.1:p.Leu473Val
|
|
|
XM_011526209.1:c.1366T>G
|
XP_011524511.1:p.Leu456Val
|
|
|
XM_011526210.1:c.1366T>G
|
XP_011524512.1:p.Leu456Val
|
|
|
XM_011526211.1:c.1366T>G
|
XP_011524513.1:p.Leu456Val
|
|
|
XM_011526212.1:c.1366T>G
|
XP_011524514.1:p.Leu456Val
|
|
|
XM_011526213.1:c.1366T>G
|
XP_011524515.1:p.Leu456Val
|
|
|
XM_011526214.1:c.1366T>G
|
XP_011524516.1:p.Leu456Val
|
|
|
NM_030632.2:c.1534T>G
|
NP_085135.1:p.Leu512Val
|
|
|
XM_011526205.2:c.1510T>G
|
XP_011524507.1:p.Leu504Val
|
|
|
XM_011526206.2:c.1456T>G
|
XP_011524508.1:p.Leu486Val
|
|
|
XM_011526213.2:c.1366T>G
|
XP_011524515.1:p.Leu456Val
|
|
|
XM_017026012.1:c.1456T>G
|
XP_016881501.1:p.Leu486Val
|
|
|
XM_017026013.1:c.1366T>G
|
XP_016881502.1:p.Leu456Val
|
|
|
XM_017026014.2:c.1366T>G
|
XP_016881503.1:p.Leu456Val
|
|
|
XM_024451269.1:c.1366T>G
|
XP_024307037.1:p.Leu456Val
|
|
|
NM_030632.3:c.1534T>G
MANE Select
|
NP_085135.1:p.Leu512Val
|
|
