ENST00000673835.1:c.1458G>T
MANE Select
|
ENSP00000501114.1:p.Trp486Cys
|
|
ENST00000361134.2:c.1458G>T
|
ENSP00000355353.2:p.Trp486Cys
|
|
ENST00000538474.5:c.1458G>T
|
ENSP00000442397.1:p.Trp486Cys
|
|
NM_001177316.1:c.1458G>T
|
NP_001170787.1:p.Trp486Cys
|
|
NM_001177317.1:c.1458G>T
|
NP_001170788.1:p.Trp486Cys
|
|
NM_080877.2:c.1458G>T
|
NP_543153.1:p.Trp486Cys
|
|
XM_011518262.1:c.*17G>T
|
XP_011516564.1:n.*17G>T
|
|
XM_017014291.1:c.*17G>T
|
XP_016869780.1:n.*17G>T
|
|
XM_017014292.1:c.1458G>T
|
XP_016869781.1:p.Trp486Cys
|
|
NM_001177316.2:c.1458G>T
MANE Select
|
NP_001170787.2:p.Trp486Cys
|
|
NM_001177317.2:c.1458G>T
|
NP_001170788.2:p.Trp486Cys
|
|
NM_080877.3:c.1458G>T
|
NP_543153.2:p.Trp486Cys
|
|