ENST00000449082.3:c.3184G=
MANE Select
|
ENSP00000390600.2:p.Gly1062=
|
|
ENST00000643924.1:c.3181G=
|
ENSP00000495595.1:p.Gly1061=
|
|
ENST00000655275.1:c.3208G=
|
ENSP00000499510.1:p.Gly1070=
|
|
ENST00000449082.2:c.3184G=
|
ENSP00000390600.2:p.Gly1062=
|
|
NM_001293306.2:c.3181G=
|
NP_001280235.2:p.Gly1061=
|
|
NM_001293307.2:c.2890G=
|
NP_001280236.2:p.Gly964=
|
|
NM_006514.3:c.3184G=
|
NP_006505.3:p.Gly1062=
|
|
XM_005265371.2:c.3193G=
|
XP_005265428.1:p.Gly1065=
|
|
XM_011533993.1:c.3190G=
|
XP_011532295.1:p.Gly1064=
|
|
XM_011533994.1:c.2899G=
|
XP_011532296.1:p.Gly967=
|
|
XM_005265371.3:c.3193G=
|
XP_005265428.1:p.Gly1065=
|
|
XM_011533993.2:c.3190G=
|
XP_011532295.1:p.Gly1064=
|
|
XM_011533994.2:c.2899G=
|
XP_011532296.1:p.Gly967=
|
|
NM_006514.4:c.3184G=
MANE Select
|
NP_006505.4:p.Gly1062=
|
|