|
NM_006736.6:c.562G>A
MANE Select
|
NP_006727.2:p.Gly188Arg
|
|
ENST00000336576.10:c.562G>A
MANE Select
|
ENSP00000338019.5:p.Gly188Arg
|
|
NM_001039550.1:c.562G>A
|
NP_001034639.1:p.Gly188Arg
|
|
NM_001039550.2:c.562G>A
|
NP_001034639.1:p.Gly188Arg
|
|
NM_006736.5:c.562G>A
|
NP_006727.2:p.Gly188Arg
|
|
ENST00000336576.9:c.562G>A
|
ENSP00000338019.5:p.Gly188Arg
|
|
ENST00000392086.8:c.562G>A
|
ENSP00000375936.4:p.Gly188Arg
|
|
ENST00000392087.6:c.469G>A
|
ENSP00000375937.2:p.Gly157Arg
|
|
ENST00000425450.5:c.562G>A
|
ENSP00000414796.1:p.Gly188Arg
|
|
ENST00000463463.5:n.553G>A
|
|
|
ENST00000472019.5:n.305G>A
|
|
|
ENST00000473750.5:n.349G>A
|
|
|
ENST00000476254.1:n.186G>A
|
|
|
ENST00000477917.5:n.2166G>A
|
|
|
ENST00000684599.1:n.769G>A
|
|