ENST00000295754.10:c.965G>C
MANE Select
|
ENSP00000295754.5:p.Trp322Ser
|
|
ENST00000672866.1:n.2561G>C
|
|
|
ENST00000295754.9:c.965G>C
|
ENSP00000295754.5:p.Trp322Ser
|
|
ENST00000359013.4:c.1040G>C
|
ENSP00000351905.4:p.Trp347Ser
|
|
NM_001024847.2:c.1040G>C , LRG_779t1:c.1040G>C
|
NP_001020018.1:p.Trp347Ser
|
|
NM_003242.5:c.965G>C
|
NP_003233.4:p.Trp322Ser
|
|
XM_011534043.1:c.992G>C
|
XP_011532345.1:p.Trp331Ser
|
|
XM_011534044.1:c.917G>C
|
XP_011532346.1:p.Trp306Ser
|
|
XM_011534045.1:c.860G>C
|
XP_011532347.1:p.Trp287Ser
|
|
XM_011534043.2:c.992G>C
|
XP_011532345.1:p.Trp331Ser
|
|
XM_011534045.3:c.860G>C
|
XP_011532347.1:p.Trp287Ser
|
|
XM_017007106.1:c.860G>C
|
XP_016862595.1:p.Trp287Ser
|
|
NM_003242.6:c.965G>C
MANE Select
|
NP_003233.4:p.Trp322Ser
|
|