ENST00000301305.8:c.1166C>G
MANE Select
|
ENSP00000301305.4:p.Thr389Arg
|
|
ENST00000276833.9:c.1091C>G
|
ENSP00000276833.5:p.Thr364Arg
|
|
ENST00000301305.7:c.1166C>G
|
ENSP00000301305.3:p.Thr389Arg
|
|
ENST00000531789.1:n.3C>G
|
|
|
NM_017767.2:c.1091C>G
|
NP_060237.2:p.Thr364Arg
|
|
NM_130849.3:c.1166C>G
|
NP_570901.2:p.Thr389Arg
|
|
XM_006716599.1:c.1166C>G
|
XP_006716662.1:p.Thr389Arg
|
|
XM_011517153.1:c.884C>G
|
XP_011515455.1:p.Thr295Arg
|
|
XM_024447188.1:c.884C>G
|
XP_024302956.1:p.Thr295Arg
|
|
XM_024447189.1:c.884C>G
|
XP_024302957.1:p.Thr295Arg
|
|
NM_001374839.1:c.884C>G
|
NP_001361768.1:p.Thr295Arg
|
|
NM_017767.3:c.1091C>G
|
NP_060237.3:p.Thr364Arg
|
|
NM_130849.4:c.1166C>G
MANE Select
|
NP_570901.3:p.Thr389Arg
|
|