ENST00000525403.6:c.*240C>G
|
ENSP00000432210.2:n.*240C>G
|
|
ENST00000698910.1:c.1337C>G
|
ENSP00000514024.1:p.Pro446Arg
|
|
ENST00000698911.1:c.1922C>G
|
ENSP00000514025.1:p.Pro641Arg
|
|
ENST00000698912.1:c.*240C>G
|
ENSP00000514026.1:n.*240C>G
|
|
ENST00000698913.1:c.1604C>G
|
ENSP00000514027.1:p.Pro535Arg
|
|
ENST00000698915.1:c.1910C>G
|
ENSP00000514029.1:p.Pro637Arg
|
|
ENST00000698916.1:c.1847C>G
|
ENSP00000514030.1:p.Pro616Arg
|
|
ENST00000698918.1:c.*1564C>G
|
ENSP00000514031.1:n.*1564C>G
|
|
ENST00000698919.1:c.*759C>G
|
ENSP00000514032.1:n.*759C>G
|
|
ENST00000698920.1:n.1126C>G
|
|
|
ENST00000526596.2:c.1919C>G
MANE Select
|
ENSP00000433266.2:p.Pro640Arg
|
|
ENST00000300737.8:c.1826C>G
|
ENSP00000300737.4:p.Pro609Arg
|
|
ENST00000526156.1:n.624C>G
|
|
|
ENST00000526596.1:c.1111C>G
|
|
|
ENST00000527651.5:c.*240C>G
|
ENSP00000436208.1:n.*240C>G
|
|
ENST00000533977.5:c.1307C>G
|
ENSP00000434767.1:p.Pro436Arg
|
|
ENST00000616714.4:c.2144C>G
|
ENSP00000478059.1:p.Pro715Arg
|
|
NM_001277961.1:c.2144C>G
|
NP_001264890.1:p.Pro715Arg
|
|
NM_001277962.1:c.*240C>G
|
NP_001264891.1:n.*240C>G
|
|
NM_003156.3:c.1826C>G , LRG_164t1:c.1826C>G
|
NP_003147.2:p.Pro609Arg
|
|
NM_001277962.2:c.*240C>G
|
NP_001264891.1:n.*240C>G
|
|
NM_001277961.3:c.2144C>G
|
NP_001264890.1:p.Pro715Arg
|
|
NM_001382566.1:c.1922C>G
|
NP_001369495.1:p.Pro641Arg
|
|
NM_001382567.1:c.1919C>G
MANE Select
|
NP_001369496.1:p.Pro640Arg
|
|
NM_001382568.1:c.1847C>G
|
NP_001369497.1:p.Pro616Arg
|
|
NM_001382569.1:c.1691C>G
|
NP_001369498.1:p.Pro564Arg
|
|
NM_001382570.1:c.1598C>G
|
NP_001369499.1:p.Pro533Arg
|
|
NM_001382571.1:c.1346C>G
|
NP_001369500.1:p.Pro449Arg
|
|
NM_001382575.1:c.1604C>G
|
NP_001369504.1:p.Pro535Arg
|
|
NM_001382576.1:c.1604C>G
|
NP_001369505.1:p.Pro535Arg
|
|
NM_001382577.1:c.1604C>G
|
NP_001369506.1:p.Pro535Arg
|
|
NM_001382578.1:c.*240C>G
|
NP_001369507.1:n.*240C>G
|
|
NM_001382579.1:c.*240C>G
|
NP_001369508.1:n.*240C>G
|
|
NM_001382580.1:c.*240C>G
|
NP_001369509.1:n.*240C>G
|
|
NM_001382581.1:c.1337C>G
|
NP_001369510.1:p.Pro446Arg
|
|
NM_003156.4:c.1826C>G
|
NP_003147.2:p.Pro609Arg
|
|
NR_168436.1:n.1750C>G
|
|
|
NR_168437.1:n.2255C>G
|
|
|
NR_168438.1:n.2077C>G
|
|
|