ENST00000681320.1:c.7858G>C
MANE Select
|
ENSP00000506558.1:p.Gly2620Arg
|
|
ENST00000328333.12:c.7858G>C
|
ENSP00000332371.8:p.Gly2620Arg
|
|
ENST00000459756.5:n.681G>C
|
|
|
ENST00000487017.5:n.4497G>C
|
|
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NM_000094.3:c.7858G>C , LRG_286t1:c.7858G>C
|
NP_000085.1:p.Gly2620Arg
|
|
XM_011533336.1:c.7885G>C
|
XP_011531638.1:p.Gly2629Arg
|
|
XM_011533337.1:c.7858G>C
|
XP_011531639.1:p.Gly2620Arg
|
|
XM_011533338.1:c.7825G>C
|
XP_011531640.1:p.Gly2609Arg
|
|
XR_940369.1:n.7921G>C
|
|
|
XR_940370.1:n.7921G>C
|
|
|
XR_940371.1:n.7921G>C
|
|
|
XM_017005688.1:c.7798G>C
|
XP_016861177.1:p.Gly2600Arg
|
|
XR_001740003.1:n.7894G>C
|
|
|
XR_001740004.1:n.7894G>C
|
|
|
XR_001740005.1:n.7894G>C
|
|
|
NM_000094.4:c.7858G>C
MANE Select
|
NP_000085.1:p.Gly2620Arg
|
|