ENST00000700485.1:n.169A=
|
|
|
ENST00000700486.1:n.207A=
|
|
|
ENST00000700487.1:n.175A=
|
|
|
ENST00000181839.10:c.2433A=
MANE Select
|
ENSP00000181839.4:p.Glu811=
|
|
ENST00000340829.10:c.2433A=
|
ENSP00000340557.5:p.Glu811=
|
|
ENST00000484589.2:c.985A=
|
|
|
ENST00000643859.1:c.1324A=
|
|
|
ENST00000643915.1:c.747A=
|
ENSP00000496187.1:p.Glu249=
|
|
ENST00000645470.1:c.363A=
|
ENSP00000495036.1:p.Glu121=
|
|
ENST00000646039.1:c.1773A=
|
ENSP00000494168.1:p.Glu591=
|
|
ENST00000647453.1:n.1502A=
|
|
|
ENST00000181839.8:c.2433A=
|
ENSP00000181839.4:p.Glu811=
|
|
ENST00000340829.9:c.2433A=
|
ENSP00000340557.5:p.Glu811=
|
|
ENST00000484589.1:n.985A=
|
|
|
ENST00000611390.1:c.591A=
|
ENSP00000484610.1:p.Glu197=
|
|
ENST00000613626.4:c.591A=
|
ENSP00000480835.1:p.Glu197=
|
|
NM_003718.4:c.2433A=
|
NP_003709.3:p.Glu811=
|
|
NM_031267.3:c.2433A=
|
NP_112557.2:p.Glu811=
|
|
XM_011515597.1:c.2433A=
|
XP_011513899.1:p.Glu811=
|
|
XM_011515598.1:c.2433A=
|
XP_011513900.1:p.Glu811=
|
|
XM_011515597.3:c.2433A=
|
XP_011513899.1:p.Glu811=
|
|
XM_017012750.2:c.2433A=
|
XP_016868239.1:p.Glu811=
|
|
XM_017012751.2:c.2433A=
|
XP_016868240.1:p.Glu811=
|
|
NM_003718.5:c.2433A=
MANE Select
|
NP_003709.3:p.Glu811=
|
|