ENST00000399408.7:c.603C>T
|
ENSP00000382340.4:p.Thr201=
|
|
ENST00000399410.8:c.603C>T
MANE Select
|
ENSP00000382342.3:p.Thr201=
|
|
ENST00000572882.3:c.603C>T
|
ENSP00000461615.2:p.Thr201=
|
|
ENST00000574224.2:n.678C>T
|
|
|
ENST00000677164.1:c.489+1981C>T
|
ENSP00000502873.1:n.489+1981C>T
|
|
ENST00000678422.1:c.603C>T
|
ENSP00000503954.1:p.Thr201=
|
|
ENST00000679043.1:n.555C>T
|
|
|
ENST00000399408.6:c.-376C>T
|
ENSP00000382340.3:n.-376C>T
|
|
ENST00000399410.7:c.603C>T
|
ENSP00000382342.3:p.Thr201=
|
|
ENST00000572882.2:c.298C>T
|
|
|
ENST00000574224.1:n.203C>T
|
|
|
NM_004996.3:c.603C>T
|
NP_004987.2:p.Thr201=
|
|
XM_011522497.1:c.579C>T
|
XP_011520799.1:p.Thr193=
|
|
XM_011522498.1:c.657C>T
|
XP_011520800.1:p.Thr219=
|
|
XM_011522498.2:c.657C>T
|
XP_011520800.1:p.Thr219=
|
|
XM_017023237.1:c.657C>T
|
XP_016878726.1:p.Thr219=
|
|
XM_017023238.1:c.543+1981C>T
|
XP_016878727.1:n.543+1981C>T
|
|
XM_017023239.1:c.519C>T
|
XP_016878728.1:p.Thr173=
|
|
XM_017023240.1:c.657C>T
|
XP_016878729.1:p.Thr219=
|
|
XM_017023241.1:c.405+6708C>T
|
XP_016878730.1:n.405+6708C>T
|
|
XM_017023242.1:c.657C>T
|
XP_016878731.1:p.Thr219=
|
|
XM_017023243.2:c.657C>T
|
XP_016878732.1:p.Thr219=
|
|
NM_004996.4:c.603C>T
MANE Select
|
NP_004987.2:p.Thr201=
|
|