ENST00000442544.7:c.482G>C
MANE Select
|
ENSP00000389140.2:p.Cys161Ser
|
|
ENST00000304775.12:c.283G>C
|
|
|
ENST00000412726.5:c.413G>C
|
ENSP00000397322.2:p.Cys138Ser
|
|
ENST00000442544.6:c.482G>C
|
ENSP00000389140.2:p.Cys161Ser
|
|
ENST00000579349.1:c.403G>C
|
|
|
ENST00000580024.1:n.395G>C
|
|
|
ENST00000581559.1:c.403G>C
|
ENSP00000463463.1:n.403G>C
|
|
NM_005215.3:c.482G>C
|
NP_005206.2:p.Cys161Ser
|
|
XM_011525843.1:c.482G>C
|
XP_011524145.1:p.Cys161Ser
|
|
XM_011525845.1:c.482G>C
|
XP_011524147.1:p.Cys161Ser
|
|
XM_011525846.1:c.482G>C
|
XP_011524148.1:p.Cys161Ser
|
|
XM_017025568.1:c.482G>C
|
XP_016881057.1:p.Cys161Ser
|
|
XM_017025569.1:c.482G>C
|
XP_016881058.1:p.Cys161Ser
|
|
NM_005215.4:c.482G>C
MANE Select
|
NP_005206.2:p.Cys161Ser
|
|