|
ENST00000342992.11:c.31741+203C>T
|
ENSP00000343764.6:n.31741+203C>T
|
|
|
ENST00000342175.11:c.13859-16485C>T
|
ENSP00000340554.6:n.13859-16485C>T
|
|
|
ENST00000359218.10:c.13658-16485C>T
|
ENSP00000352154.5:n.13658-16485C>T
|
|
|
ENST00000342175.10:c.13859-16485C>T
|
ENSP00000340554.6:n.13859-16485C>T
|
|
|
ENST00000342992.10:c.31741+203C>T
|
ENSP00000343764.6:n.31741+203C>T
|
|
|
ENST00000359218.9:c.13658-16485C>T
|
ENSP00000352154.5:n.13658-16485C>T
|
|
|
ENST00000414766.5:c.2440+14831C>T
|
ENSP00000401501.1:n.2440+14831C>T
|
|
|
ENST00000460472.6:c.13283-16485C>T
|
ENSP00000434586.1:n.13283-16485C>T
|
|
|
ENST00000589042.5:c.37454-8C>T
MANE Select
|
ENSP00000467141.1:n.37454-8C>T
|
|
|
ENST00000591111.5:c.34265-8C>T
|
ENSP00000465570.1:n.34265-8C>T
|
|
|
ENST00000615779.4:c.34522+203C>T
|
ENSP00000483597.1:n.34522+203C>T
|
|
|
NM_001256850.1:c.34522+203C>T
|
NP_001243779.1:n.34522+203C>T
|
|
|
NM_001267550.2:c.37454-8C>T
MANE Select
|
NP_001254479.2:n.37454-8C>T
|
|
|
NM_003319.4:c.13283-16485C>T
|
NP_003310.4:n.13283-16485C>T
|
|
|
NM_133378.4:c.31741+203C>T
|
NP_596869.4:n.31741+203C>T
|
|
|
NM_133432.3:c.13658-16485C>T
|
NP_597676.3:n.13658-16485C>T
|
|
|
NM_133437.4:c.13859-16485C>T
|
NP_597681.4:n.13859-16485C>T
|
|
|
XM_011511729.1:c.36551-8C>T
|
XP_011510031.1:n.36551-8C>T
|
|
|
XM_011511730.1:c.13469-16485C>T
|
XP_011510032.1:n.13469-16485C>T
|
|
|
XM_011511731.1:c.13328-16485C>T
|
XP_011510033.1:n.13328-16485C>T
|
|
|
XM_017004819.1:c.36347-8C>T
|
XP_016860308.1:n.36347-8C>T
|
|
|
XM_017004820.1:c.31745-8C>T
|
XP_016860309.1:n.31745-8C>T
|
|
|
XM_017004821.1:c.31742-8C>T
|
XP_016860310.1:n.31742-8C>T
|
|
|
XM_017004822.1:c.31858+14831C>T
|
XP_016860311.1:n.31858+14831C>T
|
|
|
XM_017004823.1:c.13424-16485C>T
|
XP_016860312.1:n.13424-16485C>T
|
|
|
XM_024453094.1:c.33389-8C>T
|
XP_024308862.1:n.33389-8C>T
|
|
|
XM_024453095.1:c.33386-8C>T
|
XP_024308863.1:n.33386-8C>T
|
|
|
XM_024453096.1:c.32819-8C>T
|
XP_024308864.1:n.32819-8C>T
|
|
|
XM_024453097.1:c.31690+14831C>T
|
XP_024308865.1:n.31690+14831C>T
|
|
|
XM_024453098.1:c.31609+14831C>T
|
XP_024308866.1:n.31609+14831C>T
|
|
|
XM_024453099.1:c.13424-16485C>T
|
XP_024308867.1:n.13424-16485C>T
|
|
|
XM_024453100.1:c.203-8C>T
|
XP_024308868.1:n.203-8C>T
|
|
