ENST00000342992.11:c.51343C>A
(TTN)
|
ENSP00000343764.6:p.Pro17115Thr
|
|
ENST00000342175.11:c.32428C>A
(TTN)
|
ENSP00000340554.6:p.Pro10810Thr
|
|
ENST00000359218.10:c.32227C>A
(TTN)
|
ENSP00000352154.5:p.Pro10743Thr
|
|
ENST00000342175.10:c.32428C>A
(TTN)
|
ENSP00000340554.6:p.Pro10810Thr
|
|
ENST00000342992.10:c.51343C>A
(TTN)
|
ENSP00000343764.6:p.Pro17115Thr
|
|
ENST00000359218.9:c.32227C>A
(TTN)
|
ENSP00000352154.5:p.Pro10743Thr
|
|
ENST00000460472.6:c.31852C>A
(TTN)
|
ENSP00000434586.1:p.Pro10618Thr
|
|
ENST00000589042.5:c.59047C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro19683Thr
|
|
ENST00000591111.5:c.54124C>A
(TTN)
|
ENSP00000465570.1:p.Pro18042Thr
|
|
ENST00000615779.4:c.54124C>A
(TTN)
|
ENSP00000483597.1:p.Pro18042Thr
|
|
NM_001256850.1:c.54124C>A
(TTN)
|
NP_001243779.1:p.Pro18042Thr
|
|
NM_001267550.2:c.59047C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Pro19683Thr
|
|
NM_003319.4:c.31852C>A
(TTN)
|
NP_003310.4:p.Pro10618Thr
|
|
NM_133378.4:c.51343C>A
(TTN)
|
NP_596869.4:p.Pro17115Thr
|
|
NM_133432.3:c.32227C>A
(TTN)
|
NP_597676.3:p.Pro10743Thr
|
|
NM_133437.4:c.32428C>A
(TTN)
|
NP_597681.4:p.Pro10810Thr
|
|
NR_038271.1:n.597-4524G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1758G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.58144C>A
(TTN)
|
XP_011510031.1:p.Pro19382Thr
|
|
XM_011511730.1:c.32038C>A
(TTN)
|
XP_011510032.1:p.Pro10680Thr
|
|
XM_011511731.1:c.31897C>A
(TTN)
|
XP_011510033.1:p.Pro10633Thr
|
|
XM_017004819.1:c.57940C>A
(TTN)
|
XP_016860308.1:p.Pro19314Thr
|
|
XM_017004820.1:c.53338C>A
(TTN)
|
XP_016860309.1:p.Pro17780Thr
|
|
XM_017004821.1:c.53335C>A
(TTN)
|
XP_016860310.1:p.Pro17779Thr
|
|
XM_017004822.1:c.50377C>A
(TTN)
|
XP_016860311.1:p.Pro16793Thr
|
|
XM_017004823.1:c.31993C>A
(TTN)
|
XP_016860312.1:p.Pro10665Thr
|
|
XM_024453094.1:c.53488C>A
(TTN)
|
XP_024308862.1:p.Pro17830Thr
|
|
XM_024453095.1:c.53485C>A
(TTN)
|
XP_024308863.1:p.Pro17829Thr
|
|
XM_024453096.1:c.52918C>A
(TTN)
|
XP_024308864.1:p.Pro17640Thr
|
|
XM_024453097.1:c.50260C>A
(TTN)
|
XP_024308865.1:p.Pro16754Thr
|
|
XM_024453098.1:c.50179C>A
(TTN)
|
XP_024308866.1:p.Pro16727Thr
|
|
XM_024453099.1:c.31942C>A
(TTN)
|
XP_024308867.1:p.Pro10648Thr
|
|
XM_024453100.1:c.21796C>A
(TTN)
|
XP_024308868.1:p.Pro7266Thr
|
|