ENST00000298139.7:c.3457C>G
MANE Select
|
ENSP00000298139.5:p.Gln1153Glu
|
|
ENST00000650667.1:c.*3071C>G
|
ENSP00000498593.1:n.*3071C>G
|
|
ENST00000298139.5:c.3457C>G
|
ENSP00000298139.5:p.Gln1153Glu
|
|
ENST00000521620.5:n.2090C>G
|
|
|
NM_000553.4:c.3457C>G , LRG_524t1:c.3457C>G
|
NP_000544.2:p.Gln1153Glu
|
|
XM_011544639.1:c.3376C>G
|
XP_011542941.1:p.Gln1126Glu
|
|
XM_011544640.1:c.1858C>G
|
XP_011542942.1:p.Gln620Glu
|
|
XR_949470.1:n.3730C>G
|
|
|
XR_949471.1:n.3730C>G
|
|
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XR_949472.1:n.3730C>G
|
|
|
XR_949643.1:n.614+1382G>C
|
|
|
NM_000553.5:c.3457C>G
|
NP_000544.2:p.Gln1153Glu
|
|
XM_011544639.3:c.3376C>G
|
XP_011542941.1:p.Gln1126Glu
|
|
XM_024447265.1:c.3247C>G
|
XP_024303033.1:p.Gln1083Glu
|
|
XR_949470.3:n.3758C>G
|
|
|
XR_949471.3:n.3758C>G
|
|
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XR_949472.3:n.3758C>G
|
|
|
NM_000553.6:c.3457C>G
MANE Select
|
NP_000544.2:p.Gln1153Glu
|
|