ENST00000565624.3:c.9778G>A
MANE Select
|
ENSP00000456500.2:p.Gly3260Arg
|
|
ENST00000437464.1:c.9694G>A
|
ENSP00000402343.1:p.Gly3232Arg
|
|
ENST00000565624.1:c.9778G>A
|
ENSP00000456500.1:p.Gly3260Arg
|
|
NM_001127464.2:c.9694G>A
|
NP_001120936.2:p.Gly3232Arg
|
|
XM_011523386.1:c.9778G>A
|
XP_011521688.1:p.Gly3260Arg
|
|
XM_011523387.1:c.9778G>A
|
XP_011521689.1:p.Gly3260Arg
|
|
XM_011523388.1:c.9778G>A
|
XP_011521690.1:p.Gly3260Arg
|
|
XM_017023784.1:c.9778G>A
|
XP_016879273.1:p.Gly3260Arg
|
|
XM_017023785.1:c.9778G>A
|
XP_016879274.1:p.Gly3260Arg
|
|
NM_001367624.1:c.9778G>A
|
NP_001354553.1:p.Gly3260Arg
|
|
NM_001367624.2:c.9778G>A
MANE Select
|
NP_001354553.1:p.Gly3260Arg
|
|