ENST00000681320.1:c.7938T>G
MANE Select
|
ENSP00000506558.1:p.Ala2646=
|
|
ENST00000328333.12:c.7938T>G
|
ENSP00000332371.8:p.Ala2646=
|
|
ENST00000459756.5:n.761T>G
|
|
|
ENST00000487017.5:n.4577T>G
|
|
|
NM_000094.3:c.7938T>G , LRG_286t1:c.7938T>G
|
NP_000085.1:p.Ala2646=
|
|
XM_011533336.1:c.7965T>G
|
XP_011531638.1:p.Ala2655=
|
|
XM_011533337.1:c.7938T>G
|
XP_011531639.1:p.Ala2646=
|
|
XM_011533338.1:c.7905T>G
|
XP_011531640.1:p.Ala2635=
|
|
XR_940369.1:n.8001T>G
|
|
|
XR_940370.1:n.8001T>G
|
|
|
XR_940371.1:n.8001T>G
|
|
|
XM_017005688.1:c.7878T>G
|
XP_016861177.1:p.Ala2626=
|
|
XR_001740003.1:n.7974T>G
|
|
|
XR_001740004.1:n.7974T>G
|
|
|
XR_001740005.1:n.7974T>G
|
|
|
NM_000094.4:c.7938T>G
MANE Select
|
NP_000085.1:p.Ala2646=
|
|