ENST00000374479.4:c.1052T=
MANE Select
|
ENSP00000363603.3:p.Phe351=
|
|
ENST00000374479.3:c.1052T=
|
ENSP00000363603.3:p.Phe351=
|
|
NM_000147.4:c.1052T=
|
NP_000138.2:p.Phe351=
|
|
XM_005245821.1:c.677T=
|
XP_005245878.1:p.Phe226=
|
|
XM_011541167.1:c.419T=
|
XP_011539469.1:p.Phe140=
|
|
XM_005245821.3:c.677T=
|
XP_005245878.1:p.Phe226=
|
|
XM_011541167.3:c.419T=
|
XP_011539469.1:p.Phe140=
|
|
XM_017000905.2:c.749T=
|
XP_016856394.1:p.Phe250=
|
|
NM_000147.5:c.1052T=
MANE Select
|
NP_000138.2:p.Phe351=
|
|
NR_174379.1:n.1230T=
|
|
|
NR_174380.1:n.1279T=
|
|
|
NR_174381.1:n.1118T=
|
|
|
NR_174382.1:n.1515T=
|
|
|