|
NM_001267550.2:c.41641C>T
MANE Select
|
NP_001254479.2:p.Arg13881Ter
|
|
ENST00000589042.5:c.41641C>T
MANE Select
|
ENSP00000467141.1:p.Arg13881Ter
|
|
NM_001256850.1:c.36718C>T
|
NP_001243779.1:p.Arg12240Ter
|
|
NM_003319.4:c.14446C>T
|
NP_003310.4:p.Arg4816Ter
|
|
NM_133378.4:c.33937C>T
|
NP_596869.4:p.Arg11313Ter
|
|
NM_133432.3:c.14821C>T
|
NP_597676.3:p.Arg4941Ter
|
|
NM_133437.4:c.15022C>T
|
NP_597681.4:p.Arg5008Ter
|
|
ENST00000342175.10:c.15022C>T
|
ENSP00000340554.6:p.Arg5008Ter
|
|
ENST00000342175.11:c.15022C>T
|
ENSP00000340554.6:p.Arg5008Ter
|
|
ENST00000342992.10:c.33937C>T
|
ENSP00000343764.6:p.Arg11313Ter
|
|
ENST00000342992.11:c.33937C>T
|
ENSP00000343764.6:p.Arg11313Ter
|
|
ENST00000359218.10:c.14821C>T
|
ENSP00000352154.5:p.Arg4941Ter
|
|
ENST00000359218.9:c.14821C>T
|
ENSP00000352154.5:p.Arg4941Ter
|
|
ENST00000460472.6:c.14446C>T
|
ENSP00000434586.1:p.Arg4816Ter
|
|
ENST00000591111.5:c.36718C>T
|
ENSP00000465570.1:p.Arg12240Ter
|
|
ENST00000615779.4:c.36718C>T
|
ENSP00000483597.1:p.Arg12240Ter
|
|
XM_011511729.1:c.40738C>T
|
XP_011510031.1:p.Arg13580Ter
|
|
XM_011511730.1:c.14632C>T
|
XP_011510032.1:p.Arg4878Ter
|
|
XM_011511731.1:c.14491C>T
|
XP_011510033.1:p.Arg4831Ter
|
|
XM_017004819.1:c.40534C>T
|
XP_016860308.1:p.Arg13512Ter
|
|
XM_017004820.1:c.35932C>T
|
XP_016860309.1:p.Arg11978Ter
|
|
XM_017004821.1:c.35929C>T
|
XP_016860310.1:p.Arg11977Ter
|
|
XM_017004822.1:c.32971C>T
|
XP_016860311.1:p.Arg10991Ter
|
|
XM_017004823.1:c.14587C>T
|
XP_016860312.1:p.Arg4863Ter
|
|
XM_024453094.1:c.36082C>T
|
XP_024308862.1:p.Arg12028Ter
|
|
XM_024453095.1:c.36079C>T
|
XP_024308863.1:p.Arg12027Ter
|
|
XM_024453096.1:c.35512C>T
|
XP_024308864.1:p.Arg11838Ter
|
|
XM_024453097.1:c.32854C>T
|
XP_024308865.1:p.Arg10952Ter
|
|
XM_024453098.1:c.32773C>T
|
XP_024308866.1:p.Arg10925Ter
|
|
XM_024453099.1:c.14536C>T
|
XP_024308867.1:p.Arg4846Ter
|
|
XM_024453100.1:c.4390C>T
|
XP_024308868.1:p.Arg1464Ter
|