ENST00000370263.9:c.812G>C
MANE Select
|
ENSP00000359285.4:p.Cys271Ser
|
|
ENST00000370263.8:c.812G>C
|
ENSP00000359285.4:p.Cys271Ser
|
|
ENST00000463705.5:n.1460G>C
|
|
|
ENST00000467563.3:n.882G>C
|
|
|
ENST00000498043.6:c.836G>C
|
|
|
ENST00000615287.4:c.599G>C
|
ENSP00000483388.1:p.Cys200Ser
|
|
ENST00000627000.1:c.*501G>C
|
ENSP00000486914.1:n.*501G>C
|
|
ENST00000630240.1:n.533G>C
|
|
|
NM_000744.6:c.812G>C
|
NP_000735.1:p.Cys271Ser
|
|
NM_001256573.1:c.284G>C
|
NP_001243502.1:p.Cys95Ser
|
|
NR_046317.1:n.1068G>C
|
|
|
XM_011528524.1:c.599G>C
|
XP_011526826.1:p.Cys200Ser
|
|
XM_017027625.2:c.284G>C
|
XP_016883114.1:p.Cys95Ser
|
|
XM_024451822.1:c.284G>C
|
XP_024307590.1:p.Cys95Ser
|
|
NM_001256573.2:c.284G>C
|
NP_001243502.1:p.Cys95Ser
|
|
NR_046317.2:n.1021G>C
|
|
|
NM_000744.7:c.812G>C
MANE Select
|
NP_000735.1:p.Cys271Ser
|
|