|
NM_005560.6:c.9235C>G
MANE Select
|
NP_005551.3:p.Arg3079Gly
|
|
ENST00000252999.7:c.9235C>G
MANE Select
|
ENSP00000252999.3:p.Arg3079Gly
|
|
NM_005560.4:c.9235C>G
|
NP_005551.3:p.Arg3079Gly
|
|
NM_005560.5:c.9235C>G
|
NP_005551.3:p.Arg3079Gly
|
|
ENST00000370691.6:n.1184C>G
|
|
|
ENST00000491036.2:n.338C>G
|
|
|
XM_006723796.2:c.9235C>G
|
XP_006723859.1:p.Arg3079Gly
|
|
XM_006723796.3:c.9235C>G
|
XP_006723859.1:p.Arg3079Gly
|
|
XM_011528818.1:c.9097C>G
|
XP_011527120.1:p.Arg3033Gly
|
|
XM_011528818.2:c.9097C>G
|
XP_011527120.1:p.Arg3033Gly
|
|
XM_011528819.1:c.8962C>G
|
XP_011527121.1:p.Arg2988Gly
|
|
XM_011528819.2:c.8962C>G
|
XP_011527121.1:p.Arg2988Gly
|
|
XR_936532.1:n.9307C>G
|
|
|
XR_936532.2:n.9306C>G
|
|