ENST00000325455.10:c.2298A>T
MANE Select
|
ENSP00000325120.5:p.Arg766Ser
|
|
ENST00000263463.9:c.1992A>T
|
ENSP00000263463.5:p.Arg664Ser
|
|
ENST00000325455.9:c.2298A>T
|
ENSP00000325120.5:p.Arg766Ser
|
|
ENST00000526300.5:c.1992A>T
|
ENSP00000436803.1:p.Arg664Ser
|
|
ENST00000528960.5:c.2181A>T
|
ENSP00000432914.1:p.Arg727Ser
|
|
ENST00000533207.5:n.1665A>T
|
|
|
ENST00000534013.5:c.516A>T
|
ENSP00000436561.1:p.Arg172Ser
|
|
ENST00000534780.5:c.2298A>T
|
ENSP00000432352.1:p.Arg766Ser
|
|
ENST00000617858.4:c.1992A>T
|
ENSP00000481227.1:p.Arg664Ser
|
|
ENST00000619228.2:c.2181A>T
|
ENSP00000482698.1:p.Arg727Ser
|
|
NM_000926.4:c.2298A>T
MANE Select
|
NP_000917.3:p.Arg766Ser
|
|
NM_001202474.3:c.1806A>T
|
NP_001189403.1:p.Arg602Ser
|
|
NM_001271161.2:c.1500A>T
|
NP_001258090.1:p.Arg500Ser
|
|
NM_001271162.1:c.516A>T
|
NP_001258091.1:p.Arg172Ser
|
|
NR_073141.2:n.2291A>T
|
|
|
NR_073142.2:n.2174A>T
|
|
|
NR_073143.2:n.1985A>T
|
|
|
XM_006718858.2:c.2298A>T
|
XP_006718921.1:p.Arg766Ser
|
|
XM_006718858.3:c.2298A>T
|
XP_006718921.1:p.Arg766Ser
|
|
NM_001271162.2:c.516A>T
|
NP_001258091.1:p.Arg172Ser
|
|
NR_073141.3:n.2305A>T
|
|
|
NR_073142.3:n.2188A>T
|
|
|
NR_073143.3:n.1999A>T
|
|
|