ENST00000374479.4:c.1052T>C
MANE Select
|
ENSP00000363603.3:p.Phe351Ser
|
|
ENST00000374479.3:c.1052T>C
|
ENSP00000363603.3:p.Phe351Ser
|
|
NM_000147.4:c.1052T>C
|
NP_000138.2:p.Phe351Ser
|
|
XM_005245821.1:c.677T>C
|
XP_005245878.1:p.Phe226Ser
|
|
XM_011541167.1:c.419T>C
|
XP_011539469.1:p.Phe140Ser
|
|
XM_005245821.3:c.677T>C
|
XP_005245878.1:p.Phe226Ser
|
|
XM_011541167.3:c.419T>C
|
XP_011539469.1:p.Phe140Ser
|
|
XM_017000905.2:c.749T>C
|
XP_016856394.1:p.Phe250Ser
|
|
NM_000147.5:c.1052T>C
MANE Select
|
NP_000138.2:p.Phe351Ser
|
|
NR_174379.1:n.1230T>C
|
|
|
NR_174380.1:n.1279T>C
|
|
|
NR_174381.1:n.1118T>C
|
|
|
NR_174382.1:n.1515T>C
|
|
|