ENST00000270357.10:c.1607T>G
MANE Select
|
ENSP00000270357.4:p.Leu536Arg
|
|
ENST00000270357.8:c.914T>G
|
ENSP00000270357.3:p.Leu305Arg
|
|
ENST00000437406.1:c.173T>G
|
ENSP00000403319.1:p.Leu58Arg
|
|
ENST00000451363.5:c.248T>G
|
ENSP00000414661.1:p.Leu83Arg
|
|
ENST00000464550.5:n.443T>G
|
|
|
ENST00000471657.1:n.410T>G
|
|
|
ENST00000481757.5:n.2541T>G
|
|
|
ENST00000486058.5:n.1720T>G
|
|
|
ENST00000493398.5:n.753T>G
|
|
|
NM_018226.4:c.1607T>G
|
NP_060696.4:p.Leu536Arg
|
|
XM_005247036.3:c.1574T>G
|
XP_005247093.1:p.Leu525Arg
|
|
NM_018226.5:c.1607T>G
|
NP_060696.4:p.Leu536Arg
|
|
XM_005247036.4:c.1574T>G
|
XP_005247093.1:p.Leu525Arg
|
|
NM_018226.6:c.1607T>G
MANE Select
|
NP_060696.4:p.Leu536Arg
|
|