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NM_018026.4:c.2494G>A
MANE Select
|
NP_060496.2:p.Gly832Arg
|
|
ENST00000320580.9:c.2494G>A
MANE Select
|
ENSP00000316454.4:p.Gly832Arg
|
|
NM_018026.3:c.2494G>A
|
NP_060496.2:p.Gly832Arg
|
|
ENST00000320580.8:c.2494G>A
|
ENSP00000316454.4:p.Gly832Arg
|
|
ENST00000524815.5:c.-123G>A
|
ENSP00000433991.1:n.-123G>A
|
|
ENST00000525798.1:n.532G>A
|
|
|
ENST00000529677.1:c.44G>A
|
|
|
ENST00000529757.5:c.1102G>A
|
ENSP00000432858.1:p.Gly368Arg
|
|
ENST00000531597.1:c.-123G>A
|
ENSP00000434012.1:n.-123G>A
|
|
XM_011545162.1:c.2173G>A
|
XP_011543464.1:p.Gly725Arg
|
|
XM_011545163.1:c.2164G>A
|
XP_011543465.1:p.Gly722Arg
|
|
XM_011545164.1:c.2155G>A
|
XP_011543466.1:p.Gly719Arg
|
|
XM_011545164.2:c.2155G>A
|
XP_011543466.1:p.Gly719Arg
|