|
NM_000918.4:c.616T>G
MANE Select
|
NP_000909.2:p.Phe206Val
|
|
ENST00000331483.9:c.616T>G
MANE Select
|
ENSP00000327801.4:p.Phe206Val
|
|
NM_000918.3:c.616T>G
|
NP_000909.2:p.Phe206Val
|
|
ENST00000331483.8:c.616T>G
|
ENSP00000327801.4:p.Phe206Val
|
|
ENST00000415593.6:c.354+4029T>G
|
ENSP00000388117.2:n.354+4029T>G
|
|
ENST00000439918.6:c.484T>G
|
ENSP00000388374.2:p.Phe162Val
|
|
ENST00000439918.7:c.484T>G
|
ENSP00000388374.2:p.Phe162Val
|
|
ENST00000466567.3:n.5400T>G
|
|
|
ENST00000467086.6:n.1229T>G
|
|
|
ENST00000471535.2:n.570T>G
|
|
|
ENST00000472244.5:n.499T>G
|
|
|
ENST00000472244.6:n.646T>G
|
|
|
ENST00000477607.6:n.688T>G
|
|
|
ENST00000477607.7:n.808T>G
|
|
|
ENST00000478034.5:n.302T>G
|
|
|
ENST00000570907.5:c.33+4031T>G
|
ENSP00000461362.1:n.33+4031T>G
|
|
ENST00000570907.6:c.616T>G
|
ENSP00000461362.2:p.Phe206Val
|
|
ENST00000571617.1:c.243+4140T>G
|
ENSP00000458300.1:n.243+4140T>G
|
|
ENST00000571617.2:c.616T>G
|
ENSP00000458300.2:p.Phe206Val
|
|
ENST00000573778.6:c.409T>G
|
ENSP00000460088.2:p.Phe137Val
|
|
ENST00000573778.7:c.*431T>G
|
ENSP00000460088.3:n.*431T>G
|
|
ENST00000574007.5:n.814T>G
|
|
|
ENST00000574007.6:n.1278T>G
|
|
|
ENST00000574914.2:c.508T>G
|
ENSP00000460612.2:p.Phe170Val
|
|
ENST00000575069.5:c.*431T>G
|
ENSP00000459211.1:n.*431T>G
|
|
ENST00000575069.6:c.*431T>G
|
ENSP00000459211.1:n.*431T>G
|
|
ENST00000576052.1:c.354+4029T>G
|
ENSP00000461791.1:n.354+4029T>G
|
|
ENST00000576052.2:c.352+4031T>G
|
ENSP00000461791.2:n.352+4031T>G
|
|
ENST00000576380.5:c.163T>G
|
ENSP00000460285.1:p.Phe55Val
|
|
ENST00000576380.6:c.*297T>G
|
ENSP00000460285.2:n.*297T>G
|
|
ENST00000576390.5:c.233+4150T>G
|
ENSP00000461718.1:n.233+4150T>G
|
|
ENST00000576390.6:c.616T>G
|
ENSP00000461718.2:p.Phe206Val
|
|
ENST00000576541.1:c.535T>G
|
ENSP00000460741.1:p.Phe179Val
|
|
ENST00000576541.2:c.*475T>G
|
ENSP00000460741.2:n.*475T>G
|
|
ENST00000679366.1:c.616T>G
|
ENSP00000506375.1:p.Phe206Val
|
|
ENST00000679396.1:n.743T>G
|
|
|
ENST00000679439.1:c.616T>G
|
ENSP00000505377.1:p.Phe206Val
|
|
ENST00000679455.1:c.*431T>G
|
ENSP00000505971.1:n.*431T>G
|
|
ENST00000679470.1:n.703T>G
|
|
|
ENST00000679628.1:n.1605T>G
|
|
|
ENST00000679688.1:c.*237T>G
|
ENSP00000505272.1:n.*237T>G
|
|
ENST00000679889.1:c.718T>G
|
ENSP00000506718.1:p.Phe240Val
|
|
ENST00000680076.1:n.714T>G
|
|
|
ENST00000680083.1:c.*350T>G
|
ENSP00000505575.1:n.*350T>G
|
|
ENST00000680105.1:c.*74T>G
|
ENSP00000506284.1:n.*74T>G
|
|
ENST00000680191.1:c.691T>G
|
ENSP00000506544.1:p.Phe231Val
|
|
ENST00000680208.1:n.720T>G
|
|
|
ENST00000680226.1:c.616T>G
|
ENSP00000505635.1:p.Phe206Val
|
|
ENST00000680259.1:c.*1117T>G
|
ENSP00000504869.1:n.*1117T>G
|
|
ENST00000680368.1:n.2135T>G
|
|
|
ENST00000680400.1:c.-354T>G
|
ENSP00000505382.1:n.-354T>G
|
|
ENST00000680416.1:c.*915T>G
|
ENSP00000506306.1:n.*915T>G
|
|
ENST00000680547.1:n.1317T>G
|
|
|
ENST00000680559.1:n.1604T>G
|
|
|
ENST00000680593.1:c.616T>G
|
ENSP00000505754.1:p.Phe206Val
|
|
ENST00000680719.1:n.802T>G
|
|
|
ENST00000680732.1:c.*74T>G
|
ENSP00000505727.1:n.*74T>G
|
|
ENST00000680799.1:n.665T>G
|
|
|
ENST00000680838.1:n.1307T>G
|
|
|
ENST00000680846.1:c.*237T>G
|
ENSP00000506612.1:n.*237T>G
|
|
ENST00000680847.1:c.616T>G
|
ENSP00000506451.1:p.Phe206Val
|
|
ENST00000680884.1:c.718T>G
|
ENSP00000505953.1:p.Phe240Val
|
|
ENST00000680909.1:c.*943T>G
|
ENSP00000505545.1:n.*943T>G
|
|
ENST00000680914.1:c.616T>G
|
ENSP00000505149.1:p.Phe206Val
|
|
ENST00000681020.1:c.616T>G
|
ENSP00000506014.1:p.Phe206Val
|
|
ENST00000681030.1:c.*869T>G
|
ENSP00000505707.1:n.*869T>G
|
|
ENST00000681031.1:c.*405T>G
|
ENSP00000505466.1:n.*405T>G
|
|
ENST00000681068.1:n.1128T>G
|
|
|
ENST00000681161.1:c.409T>G
|
ENSP00000505659.1:p.Phe137Val
|
|
ENST00000681420.1:c.616T>G
|
ENSP00000505993.1:p.Phe206Val
|
|
ENST00000681485.1:n.853T>G
|
|
|
ENST00000681515.1:c.*128T>G
|
ENSP00000505872.1:n.*128T>G
|
|
ENST00000681566.1:c.616T>G
|
ENSP00000506218.1:p.Phe206Val
|
|
ENST00000681571.1:n.1373T>G
|
|
|
ENST00000681614.1:n.1010T>G
|
|
|
ENST00000681693.1:c.535T>G
|
ENSP00000505096.1:p.Phe179Val
|
|
ENST00000681760.1:c.*431T>G
|
ENSP00000506555.1:n.*431T>G
|
|
ENST00000681835.1:n.1962T>G
|
|
|
ENST00000681872.1:n.903T>G
|
|
|
ENST00000681933.1:c.*433T>G
|
ENSP00000504864.1:n.*433T>G
|
|
ENST00000681954.1:n.1348T>G
|
|
|
XM_024450777.1:c.616T>G
|
XP_024306545.1:p.Phe206Val
|
|
XR_002958014.1:n.680T>G
|
|
