ENST00000344327.8:c.1508T>G
MANE Select
|
ENSP00000340913.3:p.Ile503Arg
|
|
ENST00000344327.7:c.1508T>G
|
ENSP00000340913.3:p.Ile503Arg
|
|
ENST00000348423.8:c.1160T>G
|
ENSP00000343672.4:p.Ile387Arg
|
|
ENST00000360497.4:c.1343T>G
|
ENSP00000353687.4:p.Ile448Arg
|
|
ENST00000532133.5:c.1508T>G
|
ENSP00000435574.1:p.Ile503Arg
|
|
NM_004621.5:c.1508T>G
|
NP_004612.2:p.Ile503Arg
|
|
XM_006718898.2:c.1508T>G
|
XP_006718961.1:p.Ile503Arg
|
|
XM_011542968.1:c.1343T>G
|
XP_011541270.1:p.Ile448Arg
|
|
XM_011542969.1:c.1508T>G
|
XP_011541271.1:p.Ile503Arg
|
|
XM_011542968.3:c.1343T>G
|
XP_011541270.1:p.Ile448Arg
|
|
XM_017018221.2:c.1160T>G
|
XP_016873710.1:p.Ile387Arg
|
|
XR_001747948.2:n.1864T>G
|
|
|
NM_004621.6:c.1508T>G
MANE Select
|
NP_004612.2:p.Ile503Arg
|
|