ENST00000295754.10:c.1195G>C
MANE Select
|
ENSP00000295754.5:p.Gly399Arg
|
|
ENST00000672866.1:n.2791G>C
|
|
|
ENST00000295754.9:c.1195G>C
|
ENSP00000295754.5:p.Gly399Arg
|
|
ENST00000359013.4:c.1270G>C
|
ENSP00000351905.4:p.Gly424Arg
|
|
NM_001024847.2:c.1270G>C , LRG_779t1:c.1270G>C
|
NP_001020018.1:p.Gly424Arg
|
|
NM_003242.5:c.1195G>C
|
NP_003233.4:p.Gly399Arg
|
|
XM_011534043.1:c.1222G>C
|
XP_011532345.1:p.Gly408Arg
|
|
XM_011534044.1:c.1147G>C
|
XP_011532346.1:p.Gly383Arg
|
|
XM_011534045.1:c.1090G>C
|
XP_011532347.1:p.Gly364Arg
|
|
XM_011534043.2:c.1222G>C
|
XP_011532345.1:p.Gly408Arg
|
|
XM_011534045.3:c.1090G>C
|
XP_011532347.1:p.Gly364Arg
|
|
XM_017007106.1:c.1090G>C
|
XP_016862595.1:p.Gly364Arg
|
|
NM_003242.6:c.1195G>C
MANE Select
|
NP_003233.4:p.Gly399Arg
|
|