ENST00000370192.8:c.734T>C
MANE Select
|
ENSP00000359211.3:p.Ile245Thr
|
|
ENST00000370192.7:c.734T>C
|
ENSP00000359211.3:p.Ile245Thr
|
|
ENST00000474241.1:n.498T>C
|
|
|
NM_000110.3:c.734T>C , LRG_722t1:c.734T>C
|
NP_000101.2:p.Ile245Thr
|
|
XM_005270562.3:c.734T>C
|
XP_005270619.2:p.Ile245Thr
|
|
XM_006710397.2:c.734T>C
|
XP_006710460.1:p.Ile245Thr
|
|
XM_006710397.3:c.734T>C
|
XP_006710460.1:p.Ile245Thr
|
|
XM_017000507.1:c.623T>C
|
XP_016855996.1:p.Ile208Thr
|
|
XM_017000508.2:c.239T>C
|
XP_016855997.1:p.Ile80Thr
|
|
XM_017000509.2:c.239T>C
|
XP_016855998.1:p.Ile80Thr
|
|
XM_017000510.1:c.239T>C
|
XP_016855999.1:p.Ile80Thr
|
|
NM_000110.4:c.734T>C
MANE Select
|
NP_000101.2:p.Ile245Thr
|
|