ENST00000342992.11:c.39167T>C
(TTN)
|
ENSP00000343764.6:p.Ile13056Thr
|
|
ENST00000342175.11:c.20252T>C
(TTN)
|
ENSP00000340554.6:p.Ile6751Thr
|
|
ENST00000359218.10:c.20051T>C
(TTN)
|
ENSP00000352154.5:p.Ile6684Thr
|
|
ENST00000342175.10:c.20252T>C
(TTN)
|
ENSP00000340554.6:p.Ile6751Thr
|
|
ENST00000342992.10:c.39167T>C
(TTN)
|
ENSP00000343764.6:p.Ile13056Thr
|
|
ENST00000359218.9:c.20051T>C
(TTN)
|
ENSP00000352154.5:p.Ile6684Thr
|
|
ENST00000460472.6:c.19676T>C
(TTN)
|
ENSP00000434586.1:p.Ile6559Thr
|
|
ENST00000589042.5:c.46871T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile15624Thr
|
|
ENST00000591111.5:c.41948T>C
(TTN)
|
ENSP00000465570.1:p.Ile13983Thr
|
|
ENST00000615779.4:c.41948T>C
(TTN)
|
ENSP00000483597.1:p.Ile13983Thr
|
|
NM_001256850.1:c.41948T>C
(TTN)
|
NP_001243779.1:p.Ile13983Thr
|
|
NM_001267550.2:c.46871T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ile15624Thr
|
|
NM_003319.4:c.19676T>C
(TTN)
|
NP_003310.4:p.Ile6559Thr
|
|
NM_133378.4:c.39167T>C
(TTN)
|
NP_596869.4:p.Ile13056Thr
|
|
NM_133432.3:c.20051T>C
(TTN)
|
NP_597676.3:p.Ile6684Thr
|
|
NM_133437.4:c.20252T>C
(TTN)
|
NP_597681.4:p.Ile6751Thr
|
|
NR_038271.1:n.1605-1074A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.45968T>C
(TTN)
|
XP_011510031.1:p.Ile15323Thr
|
|
XM_011511730.1:c.19862T>C
(TTN)
|
XP_011510032.1:p.Ile6621Thr
|
|
XM_011511731.1:c.19721T>C
(TTN)
|
XP_011510033.1:p.Ile6574Thr
|
|
XM_017004819.1:c.45764T>C
(TTN)
|
XP_016860308.1:p.Ile15255Thr
|
|
XM_017004820.1:c.41162T>C
(TTN)
|
XP_016860309.1:p.Ile13721Thr
|
|
XM_017004821.1:c.41159T>C
(TTN)
|
XP_016860310.1:p.Ile13720Thr
|
|
XM_017004822.1:c.38201T>C
(TTN)
|
XP_016860311.1:p.Ile12734Thr
|
|
XM_017004823.1:c.19817T>C
(TTN)
|
XP_016860312.1:p.Ile6606Thr
|
|
XM_024453094.1:c.41312T>C
(TTN)
|
XP_024308862.1:p.Ile13771Thr
|
|
XM_024453095.1:c.41309T>C
(TTN)
|
XP_024308863.1:p.Ile13770Thr
|
|
XM_024453096.1:c.40742T>C
(TTN)
|
XP_024308864.1:p.Ile13581Thr
|
|
XM_024453097.1:c.38084T>C
(TTN)
|
XP_024308865.1:p.Ile12695Thr
|
|
XM_024453098.1:c.38003T>C
(TTN)
|
XP_024308866.1:p.Ile12668Thr
|
|
XM_024453099.1:c.19766T>C
(TTN)
|
XP_024308867.1:p.Ile6589Thr
|
|
XM_024453100.1:c.9620T>C
(TTN)
|
XP_024308868.1:p.Ile3207Thr
|
|