ENST00000374479.4:c.1088G>T
MANE Select
|
ENSP00000363603.3:p.Ser363Ile
|
|
ENST00000374479.3:c.1088G>T
|
ENSP00000363603.3:p.Ser363Ile
|
|
NM_000147.4:c.1088G>T
|
NP_000138.2:p.Ser363Ile
|
|
XM_005245821.1:c.713G>T
|
XP_005245878.1:p.Ser238Ile
|
|
XM_011541167.1:c.455G>T
|
XP_011539469.1:p.Ser152Ile
|
|
XM_005245821.3:c.713G>T
|
XP_005245878.1:p.Ser238Ile
|
|
XM_011541167.3:c.455G>T
|
XP_011539469.1:p.Ser152Ile
|
|
XM_017000905.2:c.785G>T
|
XP_016856394.1:p.Ser262Ile
|
|
NM_000147.5:c.1088G>T
MANE Select
|
NP_000138.2:p.Ser363Ile
|
|
NR_174379.1:n.1266G>T
|
|
|
NR_174380.1:n.1315G>T
|
|
|
NR_174381.1:n.1154G>T
|
|
|
NR_174382.1:n.1551G>T
|
|
|