ENST00000374479.4:c.1091T>C
MANE Select
|
ENSP00000363603.3:p.Ile364Thr
|
|
ENST00000374479.3:c.1091T>C
|
ENSP00000363603.3:p.Ile364Thr
|
|
NM_000147.4:c.1091T>C
|
NP_000138.2:p.Ile364Thr
|
|
XM_005245821.1:c.716T>C
|
XP_005245878.1:p.Ile239Thr
|
|
XM_011541167.1:c.458T>C
|
XP_011539469.1:p.Ile153Thr
|
|
XM_005245821.3:c.716T>C
|
XP_005245878.1:p.Ile239Thr
|
|
XM_011541167.3:c.458T>C
|
XP_011539469.1:p.Ile153Thr
|
|
XM_017000905.2:c.788T>C
|
XP_016856394.1:p.Ile263Thr
|
|
NM_000147.5:c.1091T>C
MANE Select
|
NP_000138.2:p.Ile364Thr
|
|
NR_174379.1:n.1269T>C
|
|
|
NR_174380.1:n.1318T>C
|
|
|
NR_174381.1:n.1157T>C
|
|
|
NR_174382.1:n.1554T>C
|
|
|