ENST00000318471.5:c.842C>G
MANE Select
|
ENSP00000315680.3:p.Thr281Arg
|
|
ENST00000541292.6:c.*107C>G
|
ENSP00000441004.1:n.*107C>G
|
|
ENST00000678002.1:c.530C>G
|
|
|
ENST00000678557.1:c.728C>G
|
ENSP00000502962.1:p.Thr243Arg
|
|
ENST00000679286.1:c.722C>G
|
ENSP00000503168.1:p.Thr241Arg
|
|
ENST00000318471.4:c.842C>G
|
ENSP00000315680.3:p.Thr281Arg
|
|
NM_000288.3:c.842C>G
|
NP_000279.1:p.Thr281Arg
|
|
XM_005267019.3:c.728C>G
|
XP_005267076.1:p.Thr243Arg
|
|
XM_006715502.1:c.548C>G
|
XP_006715565.1:p.Thr183Arg
|
|
XM_011535900.1:c.565C>G
|
XP_011534202.1:p.Gln189Glu
|
|
XM_005267019.4:c.728C>G
|
XP_005267076.1:p.Thr243Arg
|
|
XM_006715502.2:c.548C>G
|
XP_006715565.1:p.Thr183Arg
|
|
XM_017010934.2:c.565C>G
|
XP_016866423.1:p.Gln189Glu
|
|
NM_000288.4:c.842C>G
MANE Select
|
NP_000279.1:p.Thr281Arg
|
|