ENST00000342992.11:c.96733A>T
(TTN)
|
ENSP00000343764.6:p.Thr32245Ser
|
|
ENST00000342175.11:c.77818A>T
(TTN)
|
ENSP00000340554.6:p.Thr25940Ser
|
|
ENST00000359218.10:c.77617A>T
(TTN)
|
ENSP00000352154.5:p.Thr25873Ser
|
|
ENST00000342175.10:c.77818A>T
(TTN)
|
ENSP00000340554.6:p.Thr25940Ser
|
|
ENST00000342992.10:c.96733A>T
(TTN)
|
ENSP00000343764.6:p.Thr32245Ser
|
|
ENST00000359218.9:c.77617A>T
(TTN)
|
ENSP00000352154.5:p.Thr25873Ser
|
|
ENST00000460472.6:c.77242A>T
(TTN)
|
ENSP00000434586.1:p.Thr25748Ser
|
|
ENST00000589042.5:c.104437A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr34813Ser
|
|
ENST00000591111.5:c.99514A>T
(TTN)
|
ENSP00000465570.1:p.Thr33172Ser
|
|
ENST00000615779.4:c.99514A>T
(TTN)
|
ENSP00000483597.1:p.Thr33172Ser
|
|
NM_001256850.1:c.99514A>T
(TTN)
|
NP_001243779.1:p.Thr33172Ser
|
|
NM_001267550.2:c.104437A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Thr34813Ser
|
|
NM_003319.4:c.77242A>T
(TTN)
|
NP_003310.4:p.Thr25748Ser
|
|
NM_133378.4:c.96733A>T
(TTN)
|
NP_596869.4:p.Thr32245Ser
|
|
NM_133432.3:c.77617A>T
(TTN)
|
NP_597676.3:p.Thr25873Ser
|
|
NM_133437.4:c.77818A>T
(TTN)
|
NP_597681.4:p.Thr25940Ser
|
|
NR_038271.1:n.446+8542T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3554T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.103534A>T
(TTN)
|
XP_011510031.1:p.Thr34512Ser
|
|
XM_011511730.1:c.77428A>T
(TTN)
|
XP_011510032.1:p.Thr25810Ser
|
|
XM_011511731.1:c.77287A>T
(TTN)
|
XP_011510033.1:p.Thr25763Ser
|
|
XM_017004819.1:c.103330A>T
(TTN)
|
XP_016860308.1:p.Thr34444Ser
|
|
XM_017004820.1:c.98728A>T
(TTN)
|
XP_016860309.1:p.Thr32910Ser
|
|
XM_017004821.1:c.98725A>T
(TTN)
|
XP_016860310.1:p.Thr32909Ser
|
|
XM_017004822.1:c.95767A>T
(TTN)
|
XP_016860311.1:p.Thr31923Ser
|
|
XM_017004823.1:c.77383A>T
(TTN)
|
XP_016860312.1:p.Thr25795Ser
|
|
XM_024453094.1:c.98878A>T
(TTN)
|
XP_024308862.1:p.Thr32960Ser
|
|
XM_024453095.1:c.98875A>T
(TTN)
|
XP_024308863.1:p.Thr32959Ser
|
|
XM_024453096.1:c.98308A>T
(TTN)
|
XP_024308864.1:p.Thr32770Ser
|
|
XM_024453097.1:c.95650A>T
(TTN)
|
XP_024308865.1:p.Thr31884Ser
|
|
XM_024453098.1:c.95569A>T
(TTN)
|
XP_024308866.1:p.Thr31857Ser
|
|
XM_024453099.1:c.77332A>T
(TTN)
|
XP_024308867.1:p.Thr25778Ser
|
|
XM_024453100.1:c.67186A>T
(TTN)
|
XP_024308868.1:p.Thr22396Ser
|
|