ENST00000295754.10:c.1381T>C
MANE Select
|
ENSP00000295754.5:p.Cys461Arg
|
|
ENST00000672866.1:n.2977T>C
|
|
|
ENST00000673203.1:n.259T>C
|
|
|
ENST00000295754.9:c.1381T>C
|
ENSP00000295754.5:p.Cys461Arg
|
|
ENST00000359013.4:c.1456T>C
|
ENSP00000351905.4:p.Cys486Arg
|
|
NM_001024847.2:c.1456T>C , LRG_779t1:c.1456T>C
|
NP_001020018.1:p.Cys486Arg
|
|
NM_003242.5:c.1381T>C
|
NP_003233.4:p.Cys461Arg
|
|
XM_011534043.1:c.1408T>C
|
XP_011532345.1:p.Cys470Arg
|
|
XM_011534044.1:c.1333T>C
|
XP_011532346.1:p.Cys445Arg
|
|
XM_011534045.1:c.1276T>C
|
XP_011532347.1:p.Cys426Arg
|
|
XM_011534043.2:c.1408T>C
|
XP_011532345.1:p.Cys470Arg
|
|
XM_011534045.3:c.1276T>C
|
XP_011532347.1:p.Cys426Arg
|
|
XM_017007106.1:c.1276T>C
|
XP_016862595.1:p.Cys426Arg
|
|
NM_003242.6:c.1381T>C
MANE Select
|
NP_003233.4:p.Cys461Arg
|
|