ENST00000342992.11:c.59926G>T
(TTN)
|
ENSP00000343764.6:p.Asp19976Tyr
|
|
ENST00000342175.11:c.41011G>T
(TTN)
|
ENSP00000340554.6:p.Asp13671Tyr
|
|
ENST00000359218.10:c.40810G>T
(TTN)
|
ENSP00000352154.5:p.Asp13604Tyr
|
|
ENST00000342175.10:c.41011G>T
(TTN)
|
ENSP00000340554.6:p.Asp13671Tyr
|
|
ENST00000342992.10:c.59926G>T
(TTN)
|
ENSP00000343764.6:p.Asp19976Tyr
|
|
ENST00000359218.9:c.40810G>T
(TTN)
|
ENSP00000352154.5:p.Asp13604Tyr
|
|
ENST00000460472.6:c.40435G>T
(TTN)
|
ENSP00000434586.1:p.Asp13479Tyr
|
|
ENST00000589042.5:c.67630G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp22544Tyr
|
|
ENST00000591111.5:c.62707G>T
(TTN)
|
ENSP00000465570.1:p.Asp20903Tyr
|
|
ENST00000615779.4:c.62707G>T
(TTN)
|
ENSP00000483597.1:p.Asp20903Tyr
|
|
NM_001256850.1:c.62707G>T
(TTN)
|
NP_001243779.1:p.Asp20903Tyr
|
|
NM_001267550.2:c.67630G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asp22544Tyr
|
|
NM_003319.4:c.40435G>T
(TTN)
|
NP_003310.4:p.Asp13479Tyr
|
|
NM_133378.4:c.59926G>T
(TTN)
|
NP_596869.4:p.Asp19976Tyr
|
|
NM_133432.3:c.40810G>T
(TTN)
|
NP_597676.3:p.Asp13604Tyr
|
|
NM_133437.4:c.41011G>T
(TTN)
|
NP_597681.4:p.Asp13671Tyr
|
|
NR_038271.1:n.596+8118C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-3005C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.66727G>T
(TTN)
|
XP_011510031.1:p.Asp22243Tyr
|
|
XM_011511730.1:c.40621G>T
(TTN)
|
XP_011510032.1:p.Asp13541Tyr
|
|
XM_011511731.1:c.40480G>T
(TTN)
|
XP_011510033.1:p.Asp13494Tyr
|
|
XM_017004819.1:c.66523G>T
(TTN)
|
XP_016860308.1:p.Asp22175Tyr
|
|
XM_017004820.1:c.61921G>T
(TTN)
|
XP_016860309.1:p.Asp20641Tyr
|
|
XM_017004821.1:c.61918G>T
(TTN)
|
XP_016860310.1:p.Asp20640Tyr
|
|
XM_017004822.1:c.58960G>T
(TTN)
|
XP_016860311.1:p.Asp19654Tyr
|
|
XM_017004823.1:c.40576G>T
(TTN)
|
XP_016860312.1:p.Asp13526Tyr
|
|
XM_024453094.1:c.62071G>T
(TTN)
|
XP_024308862.1:p.Asp20691Tyr
|
|
XM_024453095.1:c.62068G>T
(TTN)
|
XP_024308863.1:p.Asp20690Tyr
|
|
XM_024453096.1:c.61501G>T
(TTN)
|
XP_024308864.1:p.Asp20501Tyr
|
|
XM_024453097.1:c.58843G>T
(TTN)
|
XP_024308865.1:p.Asp19615Tyr
|
|
XM_024453098.1:c.58762G>T
(TTN)
|
XP_024308866.1:p.Asp19588Tyr
|
|
XM_024453099.1:c.40525G>T
(TTN)
|
XP_024308867.1:p.Asp13509Tyr
|
|
XM_024453100.1:c.30379G>T
(TTN)
|
XP_024308868.1:p.Asp10127Tyr
|
|