ENST00000377075.3:c.529G>C
MANE Select
|
ENSP00000366275.2:p.Gly177Arg
|
|
ENST00000377075.2:c.529G>C
|
ENSP00000366275.2:p.Gly177Arg
|
|
NM_020184.3:c.529G>C
|
NP_064569.3:p.Gly177Arg
|
|
XM_005263914.2:c.529G>C
|
XP_005263971.1:p.Gly177Arg
|
|
XM_005263915.2:c.529G>C
|
XP_005263972.1:p.Gly177Arg
|
|
XM_011510955.1:c.529G>C
|
XP_011509257.1:p.Gly177Arg
|
|
XM_011510956.1:c.529G>C
|
XP_011509258.1:p.Gly177Arg
|
|
XM_005263914.4:c.529G>C
|
XP_005263971.1:p.Gly177Arg
|
|
XM_005263915.4:c.529G>C
|
XP_005263972.1:p.Gly177Arg
|
|
XM_011510955.3:c.529G>C
|
XP_011509257.1:p.Gly177Arg
|
|
XM_011510956.3:c.529G>C
|
XP_011509258.1:p.Gly177Arg
|
|
NM_020184.4:c.529G>C
MANE Select
|
NP_064569.3:p.Gly177Arg
|
|