ENST00000342992.11:c.96659G>T
(TTN)
|
ENSP00000343764.6:p.Ser32220Ile
|
|
ENST00000342175.11:c.77744G>T
(TTN)
|
ENSP00000340554.6:p.Ser25915Ile
|
|
ENST00000359218.10:c.77543G>T
(TTN)
|
ENSP00000352154.5:p.Ser25848Ile
|
|
ENST00000342175.10:c.77744G>T
(TTN)
|
ENSP00000340554.6:p.Ser25915Ile
|
|
ENST00000342992.10:c.96659G>T
(TTN)
|
ENSP00000343764.6:p.Ser32220Ile
|
|
ENST00000359218.9:c.77543G>T
(TTN)
|
ENSP00000352154.5:p.Ser25848Ile
|
|
ENST00000460472.6:c.77168G>T
(TTN)
|
ENSP00000434586.1:p.Ser25723Ile
|
|
ENST00000589042.5:c.104363G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34788Ile
|
|
ENST00000591111.5:c.99440G>T
(TTN)
|
ENSP00000465570.1:p.Ser33147Ile
|
|
ENST00000615779.4:c.99440G>T
(TTN)
|
ENSP00000483597.1:p.Ser33147Ile
|
|
NM_001256850.1:c.99440G>T
(TTN)
|
NP_001243779.1:p.Ser33147Ile
|
|
NM_001267550.2:c.104363G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34788Ile
|
|
NM_003319.4:c.77168G>T
(TTN)
|
NP_003310.4:p.Ser25723Ile
|
|
NM_133378.4:c.96659G>T
(TTN)
|
NP_596869.4:p.Ser32220Ile
|
|
NM_133432.3:c.77543G>T
(TTN)
|
NP_597676.3:p.Ser25848Ile
|
|
NM_133437.4:c.77744G>T
(TTN)
|
NP_597681.4:p.Ser25915Ile
|
|
NR_038271.1:n.446+8616C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3480C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.103460G>T
(TTN)
|
XP_011510031.1:p.Ser34487Ile
|
|
XM_011511730.1:c.77354G>T
(TTN)
|
XP_011510032.1:p.Ser25785Ile
|
|
XM_011511731.1:c.77213G>T
(TTN)
|
XP_011510033.1:p.Ser25738Ile
|
|
XM_017004819.1:c.103256G>T
(TTN)
|
XP_016860308.1:p.Ser34419Ile
|
|
XM_017004820.1:c.98654G>T
(TTN)
|
XP_016860309.1:p.Ser32885Ile
|
|
XM_017004821.1:c.98651G>T
(TTN)
|
XP_016860310.1:p.Ser32884Ile
|
|
XM_017004822.1:c.95693G>T
(TTN)
|
XP_016860311.1:p.Ser31898Ile
|
|
XM_017004823.1:c.77309G>T
(TTN)
|
XP_016860312.1:p.Ser25770Ile
|
|
XM_024453094.1:c.98804G>T
(TTN)
|
XP_024308862.1:p.Ser32935Ile
|
|
XM_024453095.1:c.98801G>T
(TTN)
|
XP_024308863.1:p.Ser32934Ile
|
|
XM_024453096.1:c.98234G>T
(TTN)
|
XP_024308864.1:p.Ser32745Ile
|
|
XM_024453097.1:c.95576G>T
(TTN)
|
XP_024308865.1:p.Ser31859Ile
|
|
XM_024453098.1:c.95495G>T
(TTN)
|
XP_024308866.1:p.Ser31832Ile
|
|
XM_024453099.1:c.77258G>T
(TTN)
|
XP_024308867.1:p.Ser25753Ile
|
|
XM_024453100.1:c.67112G>T
(TTN)
|
XP_024308868.1:p.Ser22371Ile
|
|