ENST00000681320.1:c.7725G>C
MANE Select
|
ENSP00000506558.1:p.Gly2575=
|
|
ENST00000328333.12:c.7725G>C
|
ENSP00000332371.8:p.Gly2575=
|
|
ENST00000459756.5:n.548G>C
|
|
|
ENST00000467985.1:n.571G>C
|
|
|
ENST00000487017.5:n.4364G>C
|
|
|
NM_000094.3:c.7725G>C , LRG_286t1:c.7725G>C
|
NP_000085.1:p.Gly2575=
|
|
XM_011533336.1:c.7752G>C
|
XP_011531638.1:p.Gly2584=
|
|
XM_011533337.1:c.7725G>C
|
XP_011531639.1:p.Gly2575=
|
|
XM_011533338.1:c.7692G>C
|
XP_011531640.1:p.Gly2564=
|
|
XM_011533339.1:c.7752G>C
|
XP_011531641.1:p.Gly2584=
|
|
XR_940369.1:n.7788G>C
|
|
|
XR_940370.1:n.7788G>C
|
|
|
XR_940371.1:n.7788G>C
|
|
|
XR_940372.1:n.7762G>C
|
|
|
XM_017005688.1:c.7665G>C
|
XP_016861177.1:p.Gly2555=
|
|
XM_017005689.1:c.7725G>C
|
XP_016861178.1:p.Gly2575=
|
|
XR_001740003.1:n.7761G>C
|
|
|
XR_001740004.1:n.7761G>C
|
|
|
XR_001740005.1:n.7761G>C
|
|
|
XR_001740006.1:n.7735G>C
|
|
|
NM_000094.4:c.7725G>C
MANE Select
|
NP_000085.1:p.Gly2575=
|
|