ENST00000262367.10:c.5557C>T
MANE Select
|
ENSP00000262367.5:p.Gln1853Ter
|
|
ENST00000262367.9:c.5557C>T
|
ENSP00000262367.5:p.Gln1853Ter
|
|
ENST00000382070.7:c.5443C>T
|
ENSP00000371502.3:p.Gln1815Ter
|
|
NM_001079846.1:c.5443C>T
|
NP_001073315.1:p.Gln1815Ter
|
|
NM_004380.2:c.5557C>T
|
NP_004371.2:p.Gln1853Ter
|
|
XM_005255124.3:c.5512C>T
|
XP_005255181.1:p.Gln1838Ter
|
|
XM_005255125.3:c.5140C>T
|
XP_005255182.1:p.Gln1714Ter
|
|
XM_006720848.2:c.5296C>T
|
XP_006720911.1:p.Gln1766Ter
|
|
XM_011522380.1:c.5503C>T
|
XP_011520682.1:p.Gln1835Ter
|
|
XM_011522381.1:c.4804C>T
|
XP_011520683.1:p.Gln1602Ter
|
|
XM_005255124.4:c.5512C>T
|
XP_005255181.1:p.Gln1838Ter
|
|
XM_005255125.4:c.5140C>T
|
XP_005255182.1:p.Gln1714Ter
|
|
XM_006720848.3:c.5296C>T
|
XP_006720911.1:p.Gln1766Ter
|
|
XM_011522381.2:c.4804C>T
|
XP_011520683.1:p.Gln1602Ter
|
|
XM_017022944.1:c.5551C>T
|
XP_016878433.1:p.Gln1851Ter
|
|
NM_004380.3:c.5557C>T
MANE Select
|
NP_004371.2:p.Gln1853Ter
|
|