ENST00000370552.8:c.1454C>T
MANE Select
|
ENSP00000359583.3:p.Thr485Ile
|
|
ENST00000370546.5:c.1454C>T
|
ENSP00000359577.1:p.Thr485Ile
|
|
ENST00000370549.5:c.1280C>T
|
ENSP00000359580.1:p.Thr427Ile
|
|
ENST00000370552.7:c.1454C>T
|
ENSP00000359583.3:p.Thr485Ile
|
|
ENST00000404542.5:c.845C>T
|
ENSP00000384384.2:p.Thr282Ile
|
|
ENST00000628193.2:c.1118C>T
|
ENSP00000485916.1:p.Thr373Ile
|
|
NM_001166244.1:c.1280C>T
|
NP_001159716.1:p.Thr427Ile
|
|
NM_001166245.1:c.1118C>T
|
NP_001159717.1:p.Thr373Ile
|
|
NM_001166246.1:c.1454C>T
|
NP_001159718.1:p.Thr485Ile
|
|
NM_021828.4:c.1454C>T
|
NP_068600.4:p.Thr485Ile
|
|
XM_006717937.2:c.938C>T
|
XP_006718000.1:p.Thr313Ile
|
|
XM_011540029.1:c.1454C>T
|
XP_011538331.1:p.Thr485Ile
|
|
XM_011540030.1:c.1292C>T
|
XP_011538332.1:p.Thr431Ile
|
|
XM_011540031.1:c.938C>T
|
XP_011538333.1:p.Thr313Ile
|
|
XM_011540033.1:c.650C>T
|
XP_011538335.1:p.Thr217Ile
|
|
XR_945794.1:n.1527C>T
|
|
|
XM_011540031.2:c.938C>T
|
XP_011538333.1:p.Thr313Ile
|
|
XM_017016495.1:c.1454C>T
|
XP_016871984.1:p.Thr485Ile
|
|
XM_017016497.1:c.938C>T
|
XP_016871986.1:p.Thr313Ile
|
|
XM_017016498.1:c.650C>T
|
XP_016871987.1:p.Thr217Ile
|
|
XM_024448119.1:c.938C>T
|
XP_024303887.1:p.Thr313Ile
|
|
XM_024448120.1:c.650C>T
|
XP_024303888.1:p.Thr217Ile
|
|
XR_001747170.1:n.1531C>T
|
|
|
NM_021828.5:c.1454C>T
MANE Select
|
NP_068600.4:p.Thr485Ile
|
|