|
ENST00000415928.6:c.665+1056C>A
|
ENSP00000388838.2:n.665+1056C>A
|
|
|
ENST00000435065.7:c.767C>A
|
ENSP00000402760.2:p.Thr256Lys
|
|
|
ENST00000448810.6:c.695C>A
|
ENSP00000401860.2:p.Thr232Lys
|
|
|
ENST00000686757.1:c.714C>A
|
ENSP00000510721.1:p.Tyr238Ter
|
|
|
ENST00000687740.1:n.1855C>A
|
|
|
|
ENST00000688151.1:n.1887C>A
|
|
|
|
ENST00000689271.1:c.671+1050C>A
|
ENSP00000510797.1:n.671+1050C>A
|
|
|
ENST00000690900.1:c.672-6C>A
|
ENSP00000510703.1:n.672-6C>A
|
|
|
ENST00000692212.1:n.521C>A
|
|
|
|
ENST00000692355.1:c.204+1069C>A
|
|
|
|
ENST00000692413.1:c.714C>A
|
ENSP00000509374.1:p.Tyr238Ter
|
|
|
ENST00000692825.1:c.763C>A
|
ENSP00000509447.1:n.763C>A
|
|
|
ENST00000693308.1:c.708C>A
|
ENSP00000509770.1:p.Tyr236Ter
|
|
|
ENST00000693763.1:n.1855C>A
|
|
|
|
ENST00000245407.8:c.695C>A
MANE Select
|
ENSP00000245407.3:p.Thr232Lys
|
|
|
ENST00000245407.7:c.695C>A
|
ENSP00000245407.3:p.Thr232Lys
|
|
|
ENST00000415928.5:c.464C>A
|
ENSP00000388838.1:p.Thr155Lys
|
|
|
ENST00000435065.6:c.767C>A
|
ENSP00000402760.2:p.Thr256Lys
|
|
|
ENST00000437841.6:c.*10C>A
|
ENSP00000400553.1:n.*10C>A
|
|
|
ENST00000448810.5:c.43C>A
|
|
|
|
ENST00000461013.5:n.8117C>A
|
|
|
|
NM_001308122.1:c.767C>A
|
NP_001295051.1:p.Thr256Lys
|
|
|
NM_003060.3:c.695C>A
|
NP_003051.1:p.Thr232Lys
|
|
|
XM_011543590.1:c.77C>A
|
XP_011541892.1:p.Thr26Lys
|
|
|
XR_427718.1:n.1055C>A
|
|
|
|
XR_948290.1:n.1036C>A
|
|
|
|
XR_948291.1:n.1049C>A
|
|
|
|
XM_011543590.2:c.77C>A
|
XP_011541892.1:p.Thr26Lys
|
|
|
XM_017009778.2:c.167C>A
|
XP_016865267.1:p.Thr56Lys
|
|
|
XR_001742215.1:n.1036C>A
|
|
|
|
XR_001742216.1:n.1055C>A
|
|
|
|
XR_427718.2:n.1055C>A
|
|
|
|
XR_948290.2:n.1036C>A
|
|
|
|
XR_948291.2:n.1049C>A
|
|
|
|
NM_003060.4:c.695C>A
MANE Select
|
NP_003051.1:p.Thr232Lys
|
|
|
NM_001308122.2:c.767C>A
|
NP_001295051.1:p.Thr256Lys
|
|
