|
NM_173855.5:c.715G>A
MANE Select
|
NP_776254.3:p.Gly239Arg
|
|
ENST00000355329.7:c.715G>A
MANE Select
|
ENSP00000347486.3:p.Gly239Arg
|
|
NM_001363685.1:c.715G>A
|
NP_001350614.1:p.Gly239Arg
|
|
NM_001363685.2:c.715G>A
|
NP_001350614.1:p.Gly239Arg
|
|
NM_173855.4:c.715G>A
|
NP_776254.3:p.Gly239Arg
|
|
ENST00000392462.6:c.*47G>A
|
ENSP00000376255.2:n.*47G>A
|
|
ENST00000542364.1:c.*47G>A
|
ENSP00000445643.1:n.*47G>A
|
|
XM_005253869.3:c.715G>A
|
XP_005253926.1:p.Gly239Arg
|
|
XM_011538213.1:c.715G>A
|
XP_011536515.1:p.Gly239Arg
|
|
XM_011538213.2:c.715G>A
|
XP_011536515.1:p.Gly239Arg
|
|
XM_011538214.1:c.370G>A
|
XP_011536516.1:p.Gly124Arg
|
|
XM_011538214.3:c.370G>A
|
XP_011536516.1:p.Gly124Arg
|
|
XR_242999.3:n.618G>A
|
|
|
XR_242999.4:n.630G>A
|
|