ENST00000391944.8:c.2162T>G
|
ENSP00000375808.4:p.Leu721Arg
|
|
ENST00000682414.1:c.2162T>G
|
ENSP00000507019.1:p.Leu721Arg
|
|
ENST00000682508.1:n.2191T>G
|
|
|
ENST00000684218.1:c.*1420T>G
|
ENSP00000507804.1:n.*1420T>G
|
|
ENST00000684264.1:n.1718T>G
|
|
|
ENST00000684407.1:c.2039T>G
|
ENSP00000507775.1:p.Leu680Arg
|
|
ENST00000684458.1:c.*648T>G
|
ENSP00000508260.1:n.*648T>G
|
|
ENST00000684468.1:n.1874T>G
|
|
|
ENST00000391945.10:c.2162T>G
MANE Select
|
ENSP00000375809.4:p.Leu721Arg
|
|
ENST00000646507.1:n.2259T>G
|
|
|
ENST00000391941.6:c.2090T>G
|
ENSP00000375805.2:p.Leu697Arg
|
|
ENST00000391942.6:n.1333T>G
|
|
|
ENST00000391944.7:c.1928T>G
|
ENSP00000375808.3:p.Leu643Arg
|
|
ENST00000391945.8:c.2162T>G
|
ENSP00000375809.3:p.Leu721Arg
|
|
ENST00000588652.5:n.2250T>G
|
|
|
NM_000400.3:c.2162T>G , LRG_461t1:c.2162T>G
|
NP_000391.1:p.Leu721Arg
|
|
XM_011526611.1:c.2084T>G
|
XP_011524913.1:p.Leu695Arg
|
|
XM_011526611.2:c.2084T>G
|
XP_011524913.1:p.Leu695Arg
|
|
XM_017026467.1:c.2039T>G
|
XP_016881956.1:p.Leu680Arg
|
|
XR_001753633.2:n.2209T>G
|
|
|
XR_001753634.2:n.2145T>G
|
|
|
NM_000400.4:c.2162T>G
MANE Select
|
NP_000391.1:p.Leu721Arg
|
|