|
ENST00000340913.11:c.1054C>T
MANE Select
|
ENSP00000341826.7:p.Arg352Ter
|
|
|
ENST00000550482.2:c.898C>T
|
ENSP00000446486.2:p.Arg300Ter
|
|
|
ENST00000676472.1:c.186C>T
|
|
|
|
ENST00000676572.1:c.280C>T
|
|
|
|
ENST00000676707.1:c.201C>T
|
|
|
|
ENST00000676725.1:n.1228C>T
|
|
|
|
ENST00000676794.1:c.73C>T
|
ENSP00000504819.1:p.Arg25Ter
|
|
|
ENST00000676853.1:c.282C>T
|
|
|
|
ENST00000676886.1:c.85-300C>T
|
|
|
|
ENST00000676951.1:c.303C>T
|
|
|
|
ENST00000677191.1:c.394C>T
|
|
|
|
ENST00000677210.1:c.1054C>T
|
ENSP00000503610.1:p.Arg352Ter
|
|
|
ENST00000677220.1:c.132+2456C>T
|
ENSP00000502987.1:n.132+2456C>T
|
|
|
ENST00000677224.1:c.156C>T
|
|
|
|
ENST00000677249.1:c.895C>T
|
ENSP00000503649.1:p.Arg299Ter
|
|
|
ENST00000677279.1:c.153C>T
|
|
|
|
ENST00000677375.1:c.898C>T
|
ENSP00000503651.1:p.Arg300Ter
|
|
|
ENST00000677385.1:c.*1240C>T
|
ENSP00000502985.1:n.*1240C>T
|
|
|
ENST00000677518.1:c.117C>T
|
|
|
|
ENST00000677539.1:c.436C>T
|
|
|
|
ENST00000677636.1:c.240C>T
|
|
|
|
ENST00000677778.1:c.75+1084C>T
|
|
|
|
ENST00000677840.1:c.147C>T
|
|
|
|
ENST00000677847.1:c.87C>T
|
|
|
|
ENST00000677945.1:c.225C>T
|
|
|
|
ENST00000678077.1:c.763C>T
|
ENSP00000504814.1:p.Arg255Ter
|
|
|
ENST00000678212.1:c.242C>T
|
|
|
|
ENST00000678279.1:n.133C>T
|
|
|
|
ENST00000678365.1:n.49-2704C>T
|
|
|
|
ENST00000678412.1:c.157-300C>T
|
|
|
|
ENST00000678418.1:n.1250C>T
|
|
|
|
ENST00000678424.1:c.279C>T
|
|
|
|
ENST00000678448.1:c.246C>T
|
ENSP00000503619.1:n.246C>T
|
|
|
ENST00000678456.1:c.76-300C>T
|
|
|
|
ENST00000678513.1:c.174C>T
|
|
|
|
ENST00000678581.1:c.282C>T
|
|
|
|
ENST00000678597.1:c.171C>T
|
|
|
|
ENST00000678611.1:c.288C>T
|
|
|
|
ENST00000678873.1:c.222C>T
|
|
|
|
ENST00000678876.1:c.240C>T
|
|
|
|
ENST00000678934.1:c.201C>T
|
|
|
|
ENST00000678970.1:c.223C>T
|
|
|
|
ENST00000679026.1:c.147C>T
|
|
|
|
ENST00000679063.1:c.222C>T
|
|
|
|
ENST00000679079.1:c.157-591C>T
|
|
|
|
ENST00000679228.1:n.1249C>T
|
|
|
|
ENST00000679273.1:c.234C>T
|
ENSP00000504626.1:n.234C>T
|
|
|
ENST00000679344.1:c.255C>T
|
|
|
|
ENST00000330752.12:c.859C>T
|
ENSP00000333504.8:p.Arg287Ter
|
|
|
ENST00000340913.10:c.1054C>T
|
ENSP00000341826.6:p.Arg352Ter
|
|
|
ENST00000546500.5:c.898C>T
|
ENSP00000448617.1:p.Arg300Ter
|
|
|
ENST00000547276.5:c.739C>T
|
ENSP00000447260.1:p.Arg247Ter
|
|
|
ENST00000547566.5:c.898C>T
|
ENSP00000449913.1:p.Arg300Ter
|
|
|
ENST00000550482.1:c.511C>T
|
ENSP00000446486.1:p.Arg171Ter
|
|
|
ENST00000551679.1:n.236C>T
|
|
|
|
NM_002136.2:c.898C>T
|
NP_002127.1:p.Arg300Ter
|
|
|
NM_031157.2:c.1054C>T
|
NP_112420.1:p.Arg352Ter
|
|
|
XM_005268826.1:c.1054C>T
|
XP_005268883.1:p.Arg352Ter
|
|
|
XR_245923.1:n.1166C>T
|
|
|
|
XR_245924.1:n.1010C>T
|
|
|
|
NM_002136.3:c.898C>T
|
NP_002127.1:p.Arg300Ter
|
|
|
NM_031157.3:c.1054C>T
|
NP_112420.1:p.Arg352Ter
|
|
|
NR_135167.1:n.1016C>T
|
|
|
|
XM_005268826.2:c.1054C>T
|
XP_005268883.1:p.Arg352Ter
|
|
|
XR_245923.2:n.1126C>T
|
|
|
|
NM_002136.4:c.898C>T
|
NP_002127.1:p.Arg300Ter
|
|
|
NM_031157.4:c.1054C>T
MANE Select
|
NP_112420.1:p.Arg352Ter
|
|
|
NR_135167.2:n.980C>T
|
|
|
