|
ENST00000380567.6:c.337C>T
|
ENSP00000369941.2:p.Gln113Ter
|
|
|
ENST00000398395.8:c.337C>T
|
ENSP00000381432.5:p.Gln113Ter
|
|
|
ENST00000464463.6:n.620C>T
|
|
|
|
ENST00000490265.6:n.199C>T
|
|
|
|
ENST00000682237.1:c.337C>T
|
ENSP00000507121.1:p.Gln113Ter
|
|
|
ENST00000682562.1:c.337C>T
|
ENSP00000507874.1:p.Gln113Ter
|
|
|
ENST00000682953.1:c.*400C>T
|
ENSP00000507878.1:n.*400C>T
|
|
|
ENST00000683055.1:c.337C>T
|
ENSP00000508191.1:p.Gln113Ter
|
|
|
ENST00000683284.1:c.159C>T
|
ENSP00000507837.1:p.Tyr53=
|
|
|
ENST00000683427.1:c.337C>T
|
ENSP00000507290.1:p.Gln113Ter
|
|
|
ENST00000683454.1:n.226C>T
|
|
|
|
ENST00000683655.1:c.337C>T
|
ENSP00000506770.1:p.Gln113Ter
|
|
|
ENST00000683713.1:c.312+2192C>T
|
ENSP00000507797.1:n.312+2192C>T
|
|
|
ENST00000684401.1:n.728C>T
|
|
|
|
ENST00000684577.1:c.337C>T
|
ENSP00000507871.1:p.Gln113Ter
|
|
|
ENST00000340096.11:c.337C>T
MANE Select
|
ENSP00000344314.6:p.Gln113Ter
|
|
|
ENST00000340096.10:c.337C>T
|
ENSP00000344314.6:p.Gln113Ter
|
|
|
ENST00000380550.6:c.337C>T
|
ENSP00000369923.3:p.Gln113Ter
|
|
|
ENST00000380567.5:c.-209C>T
|
ENSP00000369941.1:n.-209C>T
|
|
|
ENST00000398395.7:c.-198C>T
|
ENSP00000381432.4:n.-198C>T
|
|
|
ENST00000466534.1:n.177C>T
|
|
|
|
ENST00000490265.5:n.648C>T
|
|
|
|
NM_003611.2:c.337C>T
|
NP_003602.1:p.Gln113Ter
|
|
|
XM_005274599.2:c.358C>T
|
XP_005274656.1:p.Gln120Ter
|
|
|
XM_005274602.2:c.358C>T
|
XP_005274659.1:p.Gln120Ter
|
|
|
XM_005274603.2:c.358C>T
|
XP_005274660.1:p.Gln120Ter
|
|
|
XM_005274604.2:c.337C>T
|
XP_005274661.1:p.Gln113Ter
|
|
|
XM_005274606.2:c.193C>T
|
XP_005274663.1:p.Gln65Ter
|
|
|
XM_011545591.1:c.358C>T
|
XP_011543893.1:p.Gln120Ter
|
|
|
XM_011545592.1:c.145C>T
|
XP_011543894.1:p.Gln49Ter
|
|
|
XM_011545593.1:c.358C>T
|
XP_011543895.1:p.Gln120Ter
|
|
|
XM_011545594.1:c.16C>T
|
XP_011543896.1:p.Gln6Ter
|
|
|
XM_011545595.1:c.16C>T
|
XP_011543897.1:p.Gln6Ter
|
|
|
XM_011545596.1:c.358C>T
|
XP_011543898.1:p.Gln120Ter
|
|
|
XM_011545597.1:c.-209C>T
|
XP_011543899.1:n.-209C>T
|
|
|
XR_247288.2:n.697C>T
|
|
|
|
NM_001330209.1:c.337C>T
|
NP_001317138.1:p.Gln113Ter
|
|
|
NM_001330210.1:c.-209C>T
|
NP_001317139.1:n.-209C>T
|
|
|
XM_005274606.4:c.193C>T
|
XP_005274663.1:p.Gln65Ter
|
|
|
XM_011545592.3:c.145C>T
|
XP_011543894.1:p.Gln49Ter
|
|
|
XM_011545594.3:c.16C>T
|
XP_011543896.1:p.Gln6Ter
|
|
|
XM_011545597.2:c.-209C>T
|
XP_011543899.1:n.-209C>T
|
|
|
XM_017029909.1:c.-209C>T
|
XP_016885398.1:n.-209C>T
|
|
|
XM_024452468.1:c.-1603C>T
|
XP_024308236.1:n.-1603C>T
|
|
|
XM_024452469.1:c.-1603C>T
|
XP_024308237.1:n.-1603C>T
|
|
|
XM_024452470.1:c.-1603C>T
|
XP_024308238.1:n.-1603C>T
|
|
|
XM_024452471.1:c.-1603C>T
|
XP_024308239.1:n.-1603C>T
|
|
|
NM_003611.3:c.337C>T
MANE Select
|
NP_003602.1:p.Gln113Ter
|
|
|
NM_001330209.2:c.337C>T
|
NP_001317138.1:p.Gln113Ter
|
|
|
NM_001330210.2:c.-209C>T
|
NP_001317139.1:n.-209C>T
|
|
