ENST00000682089.1:n.312C>G
|
|
|
ENST00000682266.1:c.542C>G
|
ENSP00000507766.1:p.Ser181Ter
|
|
ENST00000682341.1:c.950C>G
|
ENSP00000508251.1:p.Ser317Ter
|
|
ENST00000682530.1:c.*924C>G
|
ENSP00000506805.1:n.*924C>G
|
|
ENST00000683197.1:c.950C>G
|
ENSP00000507641.1:p.Ser317Ter
|
|
ENST00000683411.1:c.542C>G
|
ENSP00000508397.1:p.Ser181Ter
|
|
ENST00000683437.1:c.542C>G
|
ENSP00000508408.1:p.Ser181Ter
|
|
ENST00000683613.1:n.1986C>G
|
|
|
ENST00000683834.1:n.1192C>G
|
|
|
ENST00000684663.1:c.947C>G
|
ENSP00000508009.1:p.Ser316Ter
|
|
ENST00000324559.9:c.992C>G
MANE Select
|
ENSP00000315371.9:p.Ser331Ter
|
|
ENST00000648804.1:n.1327C>G
|
|
|
ENST00000324559.8:c.992C>G
|
ENSP00000315371.8:p.Ser331Ter
|
|
NM_001142649.1:c.989C>G
|
NP_001136121.1:p.Ser330Ter
|
|
NM_213599.2:c.992C>G , LRG_868t1:c.992C>G
|
NP_998764.1:p.Ser331Ter
|
|
XM_005252820.2:c.950C>G
|
XP_005252877.2:p.Ser317Ter
|
|
XM_005252821.2:c.947C>G
|
XP_005252878.2:p.Ser316Ter
|
|
XM_005252822.3:c.914C>G
|
XP_005252879.1:p.Ser305Ter
|
|
XM_005252823.3:c.911C>G
|
XP_005252880.1:p.Ser304Ter
|
|
XM_011519949.1:c.899C>G
|
XP_011518251.1:p.Ser300Ter
|
|
XM_005252820.3:c.950C>G
|
XP_005252877.2:p.Ser317Ter
|
|
XM_005252821.3:c.947C>G
|
XP_005252878.2:p.Ser316Ter
|
|
XM_005252822.4:c.914C>G
|
XP_005252879.1:p.Ser305Ter
|
|
XM_011519949.2:c.899C>G
|
XP_011518251.1:p.Ser300Ter
|
|
NM_001142649.2:c.989C>G
|
NP_001136121.1:p.Ser330Ter
|
|
NM_213599.3:c.992C>G
MANE Select
|
NP_998764.1:p.Ser331Ter
|
|