|
NM_015346.4:c.6659T>A
MANE Select
|
NP_056161.2:p.Leu2220Ter
|
|
ENST00000347230.9:c.6659T>A
MANE Select
|
ENSP00000251119.5:p.Leu2220Ter
|
|
NM_015346.3:c.6659T>A
|
NP_056161.2:p.Leu2220Ter
|
|
ENST00000347230.8:c.6659T>A
|
ENSP00000251119.5:p.Leu2220Ter
|
|
ENST00000394455.6:n.1922T>A
|
|
|
ENST00000554523.5:n.7414T>A
|
|
|
ENST00000554557.5:c.*4637T>A
|
ENSP00000450431.1:n.*4637T>A
|
|
ENST00000554783.1:n.347T>A
|
|
|
ENST00000557306.1:c.197T>A
|
ENSP00000452142.1:p.Leu66Ter
|
|
ENST00000676512.1:c.6677T>A
|
ENSP00000504552.1:p.Leu2226Ter
|
|
ENST00000676620.1:c.6581T>A
|
ENSP00000504587.1:p.Leu2194Ter
|
|
ENST00000678386.1:c.6704T>A
|
ENSP00000503677.1:p.Leu2235Ter
|
|
XM_006720093.2:c.6659T>A
|
XP_006720156.1:p.Leu2220Ter
|
|
XM_011536606.1:c.5150T>A
|
XP_011534908.1:p.Leu1717Ter
|
|
XM_011536607.1:c.4334T>A
|
XP_011534909.1:p.Leu1445Ter
|
|
XM_011536608.1:c.4241T>A
|
XP_011534910.1:p.Leu1414Ter
|
|
XM_017021124.1:c.6677T>A
|
XP_016876613.1:p.Leu2226Ter
|
|
XM_017021125.1:c.6677T>A
|
XP_016876614.1:p.Leu2226Ter
|
|
XM_017021126.1:c.5168T>A
|
XP_016876615.1:p.Leu1723Ter
|
|
XM_017021127.2:c.4352T>A
|
XP_016876616.1:p.Leu1451Ter
|
|
XM_017021128.1:c.4259T>A
|
XP_016876617.1:p.Leu1420Ter
|