ENST00000681320.1:c.8473G>C
MANE Select
|
ENSP00000506558.1:p.Gly2825Arg
|
|
ENST00000328333.12:c.8473G>C
|
ENSP00000332371.8:p.Gly2825Arg
|
|
ENST00000487017.5:n.5112G>C
|
|
|
NM_000094.3:c.8473G>C , LRG_286t1:c.8473G>C
|
NP_000085.1:p.Gly2825Arg
|
|
XM_011533336.1:c.8500G>C
|
XP_011531638.1:p.Gly2834Arg
|
|
XM_011533337.1:c.8473G>C
|
XP_011531639.1:p.Gly2825Arg
|
|
XM_011533338.1:c.8440G>C
|
XP_011531640.1:p.Gly2814Arg
|
|
XR_940369.1:n.8536G>C
|
|
|
XR_940370.1:n.8536G>C
|
|
|
XR_940371.1:n.8536G>C
|
|
|
XM_017005688.1:c.8413G>C
|
XP_016861177.1:p.Gly2805Arg
|
|
XR_001740003.1:n.8509G>C
|
|
|
XR_001740004.1:n.8509G>C
|
|
|
XR_001740005.1:n.8509G>C
|
|
|
NM_000094.4:c.8473G>C
MANE Select
|
NP_000085.1:p.Gly2825Arg
|
|