ENST00000337299.7:c.3118C>T
|
ENSP00000338213.6:p.Gln1040Ter
|
|
ENST00000380518.8:c.3325C>T
MANE Select
|
ENSP00000369889.3:p.Gln1109Ter
|
|
ENST00000337299.6:c.3118C>T
|
ENSP00000338213.6:p.Gln1040Ter
|
|
ENST00000380518.7:c.3325C>T
|
ENSP00000369889.3:p.Gln1109Ter
|
|
ENST00000493991.5:n.2411C>T
|
|
|
ENST00000546974.1:n.178C>T
|
|
|
NM_001844.4:c.3325C>T
|
NP_001835.3:p.Gln1109Ter
|
|
NM_033150.2:c.3118C>T
|
NP_149162.2:p.Gln1040Ter
|
|
XM_006719242.2:c.3469C>T
|
XP_006719305.2:p.Gln1157Ter
|
|
XM_011537928.1:c.3469C>T
|
XP_011536230.1:p.Gln1157Ter
|
|
XM_011537929.1:c.3469C>T
|
XP_011536231.1:p.Gln1157Ter
|
|
XM_011537930.1:c.3469C>T
|
XP_011536232.1:p.Gln1157Ter
|
|
XM_011537931.1:c.3469C>T
|
XP_011536233.1:p.Gln1157Ter
|
|
XM_011537932.1:c.3469C>T
|
XP_011536234.1:p.Gln1157Ter
|
|
XM_011537933.1:c.3469C>T
|
XP_011536235.1:p.Gln1157Ter
|
|
XM_011537934.1:c.3466C>T
|
XP_011536236.1:p.Gln1156Ter
|
|
XM_011537935.1:c.2413C>T
|
XP_011536237.1:p.Gln805Ter
|
|
XM_017018828.1:c.3469C>T
|
XP_016874317.1:p.Gln1157Ter
|
|
XM_017018829.1:c.3466C>T
|
XP_016874318.1:p.Gln1156Ter
|
|
XM_017018830.1:c.3259C>T
|
XP_016874319.1:p.Gln1087Ter
|
|
XM_017018831.2:c.2779C>T
|
XP_016874320.1:p.Gln927Ter
|
|
NM_001844.5:c.3325C>T
MANE Select
|
NP_001835.3:p.Gln1109Ter
|
|
NM_033150.3:c.3118C>T
|
NP_149162.2:p.Gln1040Ter
|
|