|
NM_001267550.2:c.106301A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asp35434Val
|
|
ENST00000589042.5:c.106301A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp35434Val
|
|
NM_001256850.1:c.101378A>T
(TTN)
|
NP_001243779.1:p.Asp33793Val
|
|
NM_003319.4:c.79106A>T
(TTN)
|
NP_003310.4:p.Asp26369Val
|
|
NM_133378.4:c.98597A>T
(TTN)
|
NP_596869.4:p.Asp32866Val
|
|
NM_133432.3:c.79481A>T
(TTN)
|
NP_597676.3:p.Asp26494Val
|
|
NM_133437.4:c.79682A>T
(TTN)
|
NP_597681.4:p.Asp26561Val
|
|
NR_038271.1:n.446+6678T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5418T>A
(TTN-AS1)
|
|
|
ENST00000342175.10:c.79682A>T
(TTN)
|
ENSP00000340554.6:p.Asp26561Val
|
|
ENST00000342175.11:c.79682A>T
(TTN)
|
ENSP00000340554.6:p.Asp26561Val
|
|
ENST00000342992.10:c.98597A>T
(TTN)
|
ENSP00000343764.6:p.Asp32866Val
|
|
ENST00000342992.11:c.98597A>T
(TTN)
|
ENSP00000343764.6:p.Asp32866Val
|
|
ENST00000359218.10:c.79481A>T
(TTN)
|
ENSP00000352154.5:p.Asp26494Val
|
|
ENST00000359218.9:c.79481A>T
(TTN)
|
ENSP00000352154.5:p.Asp26494Val
|
|
ENST00000460472.6:c.79106A>T
(TTN)
|
ENSP00000434586.1:p.Asp26369Val
|
|
ENST00000591111.5:c.101378A>T
(TTN)
|
ENSP00000465570.1:p.Asp33793Val
|
|
ENST00000615779.4:c.101378A>T
(TTN)
|
ENSP00000483597.1:p.Asp33793Val
|
|
XM_011511729.1:c.105398A>T
(TTN)
|
XP_011510031.1:p.Asp35133Val
|
|
XM_011511730.1:c.79292A>T
(TTN)
|
XP_011510032.1:p.Asp26431Val
|
|
XM_011511731.1:c.79151A>T
(TTN)
|
XP_011510033.1:p.Asp26384Val
|
|
XM_017004819.1:c.105194A>T
(TTN)
|
XP_016860308.1:p.Asp35065Val
|
|
XM_017004820.1:c.100592A>T
(TTN)
|
XP_016860309.1:p.Asp33531Val
|
|
XM_017004821.1:c.100589A>T
(TTN)
|
XP_016860310.1:p.Asp33530Val
|
|
XM_017004822.1:c.97631A>T
(TTN)
|
XP_016860311.1:p.Asp32544Val
|
|
XM_017004823.1:c.79247A>T
(TTN)
|
XP_016860312.1:p.Asp26416Val
|
|
XM_024453094.1:c.100742A>T
(TTN)
|
XP_024308862.1:p.Asp33581Val
|
|
XM_024453095.1:c.100739A>T
(TTN)
|
XP_024308863.1:p.Asp33580Val
|
|
XM_024453096.1:c.100172A>T
(TTN)
|
XP_024308864.1:p.Asp33391Val
|
|
XM_024453097.1:c.97514A>T
(TTN)
|
XP_024308865.1:p.Asp32505Val
|
|
XM_024453098.1:c.97433A>T
(TTN)
|
XP_024308866.1:p.Asp32478Val
|
|
XM_024453099.1:c.79196A>T
(TTN)
|
XP_024308867.1:p.Asp26399Val
|
|
XM_024453100.1:c.69050A>T
(TTN)
|
XP_024308868.1:p.Asp23017Val
|
