ENST00000378585.7:c.136G>C
MANE Select
|
ENSP00000367848.4:p.Gly46Arg
|
|
ENST00000638411.1:c.136G>C
|
ENSP00000491632.1:p.Gly46Arg
|
|
ENST00000638604.1:n.200G>C
|
|
|
ENST00000638771.1:c.136G>C
|
ENSP00000492435.1:p.Gly46Arg
|
|
ENST00000639045.1:c.*122G>C
|
ENSP00000491997.1:n.*122G>C
|
|
ENST00000639777.1:n.740G>C
|
|
|
ENST00000639935.1:n.173G>C
|
|
|
ENST00000640030.1:c.76G>C
|
ENSP00000491411.1:p.Gly26Arg
|
|
ENST00000640067.1:c.136G>C
|
ENSP00000491844.1:p.Gly46Arg
|
|
ENST00000640423.1:n.145G>C
|
|
|
ENST00000640949.1:c.136G>C
|
ENSP00000492500.1:p.Gly46Arg
|
|
ENST00000378585.5:c.136G>C
|
ENSP00000367848.4:p.Gly46Arg
|
|
NM_000815.4:c.136G>C
|
NP_000806.2:p.Gly46Arg
|
|
XM_011541194.1:c.175G>C
|
XP_011539496.1:p.Gly59Arg
|
|
XM_011541194.3:c.175G>C
|
XP_011539496.1:p.Gly59Arg
|
|
XM_017000936.1:c.841G>C
|
XP_016856425.1:p.Gly281Arg
|
|
NM_000815.5:c.136G>C
MANE Select
|
NP_000806.2:p.Gly46Arg
|
|