|
NM_182943.3:c.1417C>T
MANE Select
|
NP_891988.1:p.Arg473Ter
|
|
ENST00000282903.10:c.1417C>T
MANE Select
|
ENSP00000282903.5:p.Arg473Ter
|
|
NM_000935.2:c.1417C>T
|
NP_000926.2:p.Arg473Ter
|
|
NM_000935.3:c.1417C>T
|
NP_000926.2:p.Arg473Ter
|
|
NM_182943.2:c.1417C>T
|
NP_891988.1:p.Arg473Ter
|
|
ENST00000282903.9:c.1417C>T
|
ENSP00000282903.5:p.Arg473Ter
|
|
ENST00000360060.7:c.1417C>T
|
ENSP00000353170.3:p.Arg473Ter
|
|
ENST00000461497.5:c.397C>T
|
ENSP00000419354.1:p.Arg133Ter
|
|
ENST00000469350.6:c.1333C>T
|
ENSP00000419963.2:p.Arg445Ter
|
|
ENST00000478436.1:n.1752C>T
|
|
|
ENST00000480704.2:c.*1181C>T
|
ENSP00000419880.1:n.*1181C>T
|
|
ENST00000494950.5:c.1252C>T
|
ENSP00000420094.1:p.Arg418Ter
|
|
ENST00000703517.1:n.579+23556C>T
|
|
|
ENST00000703518.1:c.1417C>T
|
ENSP00000515350.1:p.Arg473Ter
|
|
ENST00000703519.1:n.1434C>T
|
|
|
ENST00000703520.1:c.1417C>T
|
ENSP00000515351.1:p.Arg473Ter
|
|
ENST00000703521.1:c.*769C>T
|
ENSP00000515352.1:n.*769C>T
|
|
ENST00000703522.1:c.1417C>T
|
ENSP00000515353.1:p.Arg473Ter
|
|
ENST00000703523.1:c.1417C>T
|
ENSP00000515354.1:p.Arg473Ter
|
|
ENST00000703524.1:n.940C>T
|
|
|
ENST00000703525.1:n.1612C>T
|
|
|
ENST00000703526.1:n.785C>T
|
|
|
ENST00000703527.1:c.1417C>T
|
ENSP00000515355.1:p.Arg473Ter
|
|
ENST00000703528.1:c.1252C>T
|
ENSP00000515356.1:p.Arg418Ter
|
|
ENST00000703529.1:n.1612C>T
|
|
|
ENST00000706626.1:c.1417C>T
|
ENSP00000516472.1:p.Arg473Ter
|
|
ENST00000706632.1:n.281C>T
|
|
|
ENST00000706634.1:n.1612C>T
|
|
|
ENST00000706635.1:c.1312C>T
|
ENSP00000516475.1:p.Arg438Ter
|
|
ENST00000706636.1:c.*769C>T
|
ENSP00000516476.1:n.*769C>T
|
|
XM_005247535.3:c.1141C>T
|
XP_005247592.1:p.Arg381Ter
|
|
XM_005247535.4:c.1141C>T
|
XP_005247592.1:p.Arg381Ter
|
|
XM_005247536.3:c.1417C>T
|
XP_005247593.1:p.Arg473Ter
|
|
XM_017006625.2:c.1141C>T
|
XP_016862114.1:p.Arg381Ter
|
|
XM_024453599.1:c.1141C>T
|
XP_024309367.1:p.Arg381Ter
|
|
XR_001740176.2:n.1612C>T
|
|
