ENST00000342992.11:c.98296T>A
(TTN)
|
ENSP00000343764.6:p.Phe32766Ile
|
|
ENST00000342175.11:c.79381T>A
(TTN)
|
ENSP00000340554.6:p.Phe26461Ile
|
|
ENST00000359218.10:c.79180T>A
(TTN)
|
ENSP00000352154.5:p.Phe26394Ile
|
|
ENST00000342175.10:c.79381T>A
(TTN)
|
ENSP00000340554.6:p.Phe26461Ile
|
|
ENST00000342992.10:c.98296T>A
(TTN)
|
ENSP00000343764.6:p.Phe32766Ile
|
|
ENST00000359218.9:c.79180T>A
(TTN)
|
ENSP00000352154.5:p.Phe26394Ile
|
|
ENST00000460472.6:c.78805T>A
(TTN)
|
ENSP00000434586.1:p.Phe26269Ile
|
|
ENST00000589042.5:c.106000T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Phe35334Ile
|
|
ENST00000591111.5:c.101077T>A
(TTN)
|
ENSP00000465570.1:p.Phe33693Ile
|
|
ENST00000615779.4:c.101077T>A
(TTN)
|
ENSP00000483597.1:p.Phe33693Ile
|
|
NM_001256850.1:c.101077T>A
(TTN)
|
NP_001243779.1:p.Phe33693Ile
|
|
NM_001267550.2:c.106000T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Phe35334Ile
|
|
NM_003319.4:c.78805T>A
(TTN)
|
NP_003310.4:p.Phe26269Ile
|
|
NM_133378.4:c.98296T>A
(TTN)
|
NP_596869.4:p.Phe32766Ile
|
|
NM_133432.3:c.79180T>A
(TTN)
|
NP_597676.3:p.Phe26394Ile
|
|
NM_133437.4:c.79381T>A
(TTN)
|
NP_597681.4:p.Phe26461Ile
|
|
NR_038271.1:n.446+6979A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5117A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105097T>A
(TTN)
|
XP_011510031.1:p.Phe35033Ile
|
|
XM_011511730.1:c.78991T>A
(TTN)
|
XP_011510032.1:p.Phe26331Ile
|
|
XM_011511731.1:c.78850T>A
(TTN)
|
XP_011510033.1:p.Phe26284Ile
|
|
XM_017004819.1:c.104893T>A
(TTN)
|
XP_016860308.1:p.Phe34965Ile
|
|
XM_017004820.1:c.100291T>A
(TTN)
|
XP_016860309.1:p.Phe33431Ile
|
|
XM_017004821.1:c.100288T>A
(TTN)
|
XP_016860310.1:p.Phe33430Ile
|
|
XM_017004822.1:c.97330T>A
(TTN)
|
XP_016860311.1:p.Phe32444Ile
|
|
XM_017004823.1:c.78946T>A
(TTN)
|
XP_016860312.1:p.Phe26316Ile
|
|
XM_024453094.1:c.100441T>A
(TTN)
|
XP_024308862.1:p.Phe33481Ile
|
|
XM_024453095.1:c.100438T>A
(TTN)
|
XP_024308863.1:p.Phe33480Ile
|
|
XM_024453096.1:c.99871T>A
(TTN)
|
XP_024308864.1:p.Phe33291Ile
|
|
XM_024453097.1:c.97213T>A
(TTN)
|
XP_024308865.1:p.Phe32405Ile
|
|
XM_024453098.1:c.97132T>A
(TTN)
|
XP_024308866.1:p.Phe32378Ile
|
|
XM_024453099.1:c.78895T>A
(TTN)
|
XP_024308867.1:p.Phe26299Ile
|
|
XM_024453100.1:c.68749T>A
(TTN)
|
XP_024308868.1:p.Phe22917Ile
|
|