ENST00000684599.1:n.1015G>C
|
|
|
ENST00000336576.10:c.808G>C
MANE Select
|
ENSP00000338019.5:p.Gly270Arg
|
|
ENST00000336576.9:c.808G>C
|
ENSP00000338019.5:p.Gly270Arg
|
|
ENST00000392086.8:c.808G>C
|
ENSP00000375936.4:p.Gly270Arg
|
|
ENST00000392087.6:c.715G>C
|
ENSP00000375937.2:p.Gly239Arg
|
|
ENST00000463463.5:n.799G>C
|
|
|
ENST00000472019.5:n.551G>C
|
|
|
ENST00000473750.5:n.595G>C
|
|
|
ENST00000476254.1:n.432G>C
|
|
|
ENST00000477917.5:n.2412G>C
|
|
|
NM_001039550.1:c.808G>C
|
NP_001034639.1:p.Gly270Arg
|
|
NM_006736.5:c.808G>C
|
NP_006727.2:p.Gly270Arg
|
|
NM_001039550.2:c.808G>C
|
NP_001034639.1:p.Gly270Arg
|
|
NM_006736.6:c.808G>C
MANE Select
|
NP_006727.2:p.Gly270Arg
|
|