ENST00000247933.9:c.757G>C
|
ENSP00000247933.4:p.Gly253Arg
|
|
ENST00000514224.2:c.757G>C
MANE Select
|
ENSP00000425081.2:p.Gly253Arg
|
|
ENST00000652070.1:n.813G>C
|
|
|
ENST00000247933.8:c.757G>C
|
ENSP00000247933.4:p.Gly253Arg
|
|
ENST00000502910.5:c.616G>C
|
ENSP00000422952.1:p.Gly206Arg
|
|
ENST00000514192.5:c.574G>C
|
ENSP00000423685.1:p.Gly192Arg
|
|
ENST00000514224.1:c.361G>C
|
ENSP00000425081.1:p.Gly121Arg
|
|
ENST00000514698.5:n.657G>C
|
|
|
NM_000203.4:c.757G>C
|
NP_000194.2:p.Gly253Arg
|
|
NR_110313.1:n.845G>C
|
|
|
XM_006713882.2:c.361G>C
|
XP_006713945.1:p.Gly121Arg
|
|
XM_011513459.1:c.616G>C
|
XP_011511761.1:p.Gly206Arg
|
|
XM_011513460.1:c.616G>C
|
XP_011511762.1:p.Gly206Arg
|
|
XM_011513461.1:c.550G>C
|
XP_011511763.1:p.Gly184Arg
|
|
XM_011513462.1:c.469G>C
|
XP_011511764.1:p.Gly157Arg
|
|
XM_011513463.1:c.469G>C
|
XP_011511765.1:p.Gly157Arg
|
|
XR_924947.1:n.826G>C
|
|
|
NM_000203.5:c.757G>C
MANE Select
|
NP_000194.2:p.Gly253Arg
|
|
NM_001363576.1:c.361G>C
|
NP_001350505.1:p.Gly121Arg
|
|
XM_011513461.2:c.550G>C
|
XP_011511763.1:p.Gly184Arg
|
|
XM_017008163.1:c.-204G>C
|
XP_016863652.1:n.-204G>C
|
|