ENST00000265631.10:c.2000C>T
MANE Select
|
ENSP00000265631.6:p.Thr667Ile
|
|
ENST00000265631.9:c.2000C>T
|
ENSP00000265631.5:p.Thr667Ile
|
|
ENST00000416240.6:c.2003C>T
|
ENSP00000400101.2:p.Thr668Ile
|
|
ENST00000494085.1:n.503C>T
|
|
|
NM_001160210.1:c.2003C>T
|
NP_001153682.1:p.Thr668Ile
|
|
NM_014251.2:c.2000C>T
|
NP_055066.1:p.Thr667Ile
|
|
NR_027662.1:n.2075C>T
|
|
|
XM_006715831.2:c.2033C>T
|
XP_006715894.1:p.Thr678Ile
|
|
XM_011515728.1:c.1148C>T
|
XP_011514030.1:p.Thr383Ile
|
|
XM_006715831.4:c.2033C>T
|
XP_006715894.1:p.Thr678Ile
|
|
XM_017011663.1:c.1991C>T
|
XP_016867152.1:p.Thr664Ile
|
|
XM_017011664.2:c.1148C>T
|
XP_016867153.1:p.Thr383Ile
|
|
XM_017011665.1:c.1148C>T
|
XP_016867154.1:p.Thr383Ile
|
|
XR_001744525.2:n.2246C>T
|
|
|
XR_002956405.1:n.2804C>T
|
|
|
NM_014251.3:c.2000C>T
MANE Select
|
NP_055066.1:p.Thr667Ile
|
|
NR_027662.2:n.2026C>T
|
|
|
NM_001160210.2:c.2003C>T
|
NP_001153682.1:p.Thr668Ile
|
|