ENST00000359271.4:c.635G>T
MANE Select
|
ENSP00000352216.2:p.Gly212Val
|
|
ENST00000359271.3:c.635G>T
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ENSP00000352216.2:p.Gly212Val
|
|
NM_030777.3:c.635G>T
|
NP_110404.1:p.Gly212Val
|
|
XM_011529060.1:c.698G>T
|
XP_011527362.1:p.Gly233Val
|
|
XM_011529061.1:c.644G>T
|
XP_011527363.1:p.Gly215Val
|
|
XM_011529062.1:c.698G>T
|
XP_011527364.1:p.Gly233Val
|
|
XM_011529063.1:c.698G>T
|
XP_011527365.1:p.Gly233Val
|
|
XM_011529064.1:c.698G>T
|
XP_011527366.1:p.Gly233Val
|
|
XM_011529065.1:c.698G>T
|
XP_011527367.1:p.Gly233Val
|
|
XR_936641.1:n.834G>T
|
|
|
XM_011529060.2:c.698G>T
|
XP_011527362.1:p.Gly233Val
|
|
XM_011529061.2:c.644G>T
|
XP_011527363.1:p.Gly215Val
|
|
XM_011529062.2:c.698G>T
|
XP_011527364.1:p.Gly233Val
|
|
XM_011529063.2:c.698G>T
|
XP_011527365.1:p.Gly233Val
|
|
XM_011529064.2:c.698G>T
|
XP_011527366.1:p.Gly233Val
|
|
XM_011529065.2:c.698G>T
|
XP_011527367.1:p.Gly233Val
|
|
XM_017028087.2:c.635G>T
|
XP_016883576.1:p.Gly212Val
|
|
XR_936641.2:n.821G>T
|
|
|
NM_030777.4:c.635G>T
MANE Select
|
NP_110404.1:p.Gly212Val
|
|