ENST00000295754.10:c.1030_1036delinsTGGGAGG
MANE Select
|
ENSP00000295754.5:p.Trp344=
|
|
ENST00000672866.1:n.2626_2632delinsTGGGAGG
|
|
|
ENST00000295754.9:c.1030_1036delinsTGGGAGG
|
ENSP00000295754.5:p.Trp344=
|
|
ENST00000359013.4:c.1105_1111delinsTGGGAGG
|
ENSP00000351905.4:p.Trp369=
|
|
NM_001024847.2:c.1105_1111delinsTGGGAGG , LRG_779t1:c.1105_1111delinsTGGGAGG
|
NP_001020018.1:p.Trp369=
|
|
NM_003242.5:c.1030_1036delinsTGGGAGG
|
NP_003233.4:p.Trp344=
|
|
XM_011534043.1:c.1057_1063delinsTGGGAGG
|
XP_011532345.1:p.Trp353=
|
|
XM_011534044.1:c.982_988delinsTGGGAGG
|
XP_011532346.1:p.Trp328=
|
|
XM_011534045.1:c.925_931delinsTGGGAGG
|
XP_011532347.1:p.Trp309=
|
|
XM_011534043.2:c.1057_1063delinsTGGGAGG
|
XP_011532345.1:p.Trp353=
|
|
XM_011534045.3:c.925_931delinsTGGGAGG
|
XP_011532347.1:p.Trp309=
|
|
XM_017007106.1:c.925_931delinsTGGGAGG
|
XP_016862595.1:p.Trp309=
|
|
NM_003242.6:c.1030_1036delinsTGGGAGG
MANE Select
|
NP_003233.4:p.Trp344=
|
|