ENST00000371757.7:c.1279C>T
MANE Select
|
ENSP00000360822.2:p.Gln427Ter
|
|
ENST00000636995.1:n.6C>T
|
|
|
ENST00000637798.1:n.18C>T
|
|
|
ENST00000674572.1:c.1120C>T
|
ENSP00000501742.1:p.Gln374Ter
|
|
ENST00000675090.1:c.1027C>T
|
ENSP00000501833.1:p.Gln343Ter
|
|
ENST00000675399.1:c.1027C>T
|
ENSP00000501932.1:p.Gln343Ter
|
|
ENST00000676421.1:c.1036C>T
|
ENSP00000502322.1:p.Gln346Ter
|
|
ENST00000263604.5:c.1180C>T
|
ENSP00000263604.4:p.Gln394Ter
|
|
ENST00000371757.6:c.1279C>T
|
ENSP00000360822.2:p.Gln427Ter
|
|
ENST00000460750.5:c.*889C>T
|
ENSP00000418777.1:n.*889C>T
|
|
ENST00000486577.6:c.1162C>T
|
ENSP00000417578.3:p.Gln388Ter
|
|
ENST00000487664.5:c.1279C>T
|
ENSP00000417851.2:p.Gln427Ter
|
|
ENST00000488444.6:c.1222C>T
|
ENSP00000419007.3:p.Gln408Ter
|
|
ENST00000490355.6:c.1222C>T
|
ENSP00000418003.3:p.Gln408Ter
|
|
ENST00000490363.3:n.1098C>T
|
|
|
ENST00000491806.6:c.1222C>T
|
ENSP00000419086.3:p.Gln408Ter
|
|
ENST00000628528.2:c.1144C>T
|
ENSP00000486374.1:p.Gln382Ter
|
|
ENST00000630792.2:c.1120C>T
|
ENSP00000486486.1:p.Gln374Ter
|
|
ENST00000631073.2:c.1222C>T
|
ENSP00000486130.1:p.Gln408Ter
|
|
NM_001272003.1:c.1144C>T
|
NP_001258932.1:p.Gln382Ter
|
|
NM_020822.2:c.1279C>T
|
NP_065873.2:p.Gln427Ter
|
|
XM_011518877.1:c.1414C>T
|
XP_011517179.1:p.Gln472Ter
|
|
XM_011518878.1:c.1423C>T
|
XP_011517180.1:p.Gln475Ter
|
|
XM_011518879.1:c.1414C>T
|
XP_011517181.1:p.Gln472Ter
|
|
XM_011518880.1:c.1180C>T
|
XP_011517182.1:p.Gln394Ter
|
|
XM_011518881.1:c.769C>T
|
XP_011517183.1:p.Gln257Ter
|
|
XM_011518877.3:c.1414C>T
|
XP_011517179.1:p.Gln472Ter
|
|
XM_011518878.3:c.1423C>T
|
XP_011517180.1:p.Gln475Ter
|
|
XM_011518879.3:c.1414C>T
|
XP_011517181.1:p.Gln472Ter
|
|
XM_011518881.3:c.769C>T
|
XP_011517183.1:p.Gln257Ter
|
|
XM_017014931.1:c.1213C>T
|
XP_016870420.1:p.Gln405Ter
|
|
XM_017014932.1:c.1036C>T
|
XP_016870421.1:p.Gln346Ter
|
|
XM_017014933.1:c.769C>T
|
XP_016870422.1:p.Gln257Ter
|
|
XM_024447617.1:c.769C>T
|
XP_024303385.1:p.Gln257Ter
|
|
XM_024447618.1:c.769C>T
|
XP_024303386.1:p.Gln257Ter
|
|
NM_020822.3:c.1279C>T
MANE Select
|
NP_065873.2:p.Gln427Ter
|
|
NM_001272003.2:c.1144C>T
|
NP_001258932.1:p.Gln382Ter
|
|