ENST00000342992.11:c.39598A>G
(TTN)
|
ENSP00000343764.6:p.Thr13200Ala
|
|
ENST00000342175.11:c.20683A>G
(TTN)
|
ENSP00000340554.6:p.Thr6895Ala
|
|
ENST00000359218.10:c.20482A>G
(TTN)
|
ENSP00000352154.5:p.Thr6828Ala
|
|
ENST00000342175.10:c.20683A>G
(TTN)
|
ENSP00000340554.6:p.Thr6895Ala
|
|
ENST00000342992.10:c.39598A>G
(TTN)
|
ENSP00000343764.6:p.Thr13200Ala
|
|
ENST00000359218.9:c.20482A>G
(TTN)
|
ENSP00000352154.5:p.Thr6828Ala
|
|
ENST00000460472.6:c.20107A>G
(TTN)
|
ENSP00000434586.1:p.Thr6703Ala
|
|
ENST00000589042.5:c.47302A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr15768Ala
|
|
ENST00000591111.5:c.42379A>G
(TTN)
|
ENSP00000465570.1:p.Thr14127Ala
|
|
ENST00000615779.4:c.42379A>G
(TTN)
|
ENSP00000483597.1:p.Thr14127Ala
|
|
NM_001256850.1:c.42379A>G
(TTN)
|
NP_001243779.1:p.Thr14127Ala
|
|
NM_001267550.2:c.47302A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr15768Ala
|
|
NM_003319.4:c.20107A>G
(TTN)
|
NP_003310.4:p.Thr6703Ala
|
|
NM_133378.4:c.39598A>G
(TTN)
|
NP_596869.4:p.Thr13200Ala
|
|
NM_133432.3:c.20482A>G
(TTN)
|
NP_597676.3:p.Thr6828Ala
|
|
NM_133437.4:c.20683A>G
(TTN)
|
NP_597681.4:p.Thr6895Ala
|
|
NR_038271.1:n.1605-1704T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.46399A>G
(TTN)
|
XP_011510031.1:p.Thr15467Ala
|
|
XM_011511730.1:c.20293A>G
(TTN)
|
XP_011510032.1:p.Thr6765Ala
|
|
XM_011511731.1:c.20152A>G
(TTN)
|
XP_011510033.1:p.Thr6718Ala
|
|
XM_017004819.1:c.46195A>G
(TTN)
|
XP_016860308.1:p.Thr15399Ala
|
|
XM_017004820.1:c.41593A>G
(TTN)
|
XP_016860309.1:p.Thr13865Ala
|
|
XM_017004821.1:c.41590A>G
(TTN)
|
XP_016860310.1:p.Thr13864Ala
|
|
XM_017004822.1:c.38632A>G
(TTN)
|
XP_016860311.1:p.Thr12878Ala
|
|
XM_017004823.1:c.20248A>G
(TTN)
|
XP_016860312.1:p.Thr6750Ala
|
|
XM_024453094.1:c.41743A>G
(TTN)
|
XP_024308862.1:p.Thr13915Ala
|
|
XM_024453095.1:c.41740A>G
(TTN)
|
XP_024308863.1:p.Thr13914Ala
|
|
XM_024453096.1:c.41173A>G
(TTN)
|
XP_024308864.1:p.Thr13725Ala
|
|
XM_024453097.1:c.38515A>G
(TTN)
|
XP_024308865.1:p.Thr12839Ala
|
|
XM_024453098.1:c.38434A>G
(TTN)
|
XP_024308866.1:p.Thr12812Ala
|
|
XM_024453099.1:c.20197A>G
(TTN)
|
XP_024308867.1:p.Thr6733Ala
|
|
XM_024453100.1:c.10051A>G
(TTN)
|
XP_024308868.1:p.Thr3351Ala
|
|