ENST00000373588.9:c.912G=
MANE Select
|
ENSP00000362690.4:p.Glu304=
|
|
ENST00000373587.3:c.264G=
|
ENSP00000362689.3:p.Glu88=
|
|
ENST00000373588.8:c.912G=
|
ENSP00000362690.4:p.Glu304=
|
|
ENST00000620110.4:c.871-1880G=
|
ENSP00000483309.1:n.871-1880G=
|
|
NM_004959.4:c.912G=
|
NP_004950.2:p.Glu304=
|
|
XM_005251871.2:c.912G=
|
XP_005251928.1:p.Glu304=
|
|
XM_005251872.3:c.651G=
|
XP_005251929.1:p.Glu217=
|
|
XM_011518455.1:c.912G=
|
XP_011516757.1:p.Glu304=
|
|
XM_011518456.1:c.870+6982G=
|
XP_011516758.1:n.870+6982G=
|
|
NM_004959.5:c.912G=
MANE Select
|
NP_004950.2:p.Glu304=
|
|