ENST00000342992.11:c.39599C>G
(TTN)
|
ENSP00000343764.6:p.Thr13200Ser
|
|
ENST00000342175.11:c.20684C>G
(TTN)
|
ENSP00000340554.6:p.Thr6895Ser
|
|
ENST00000359218.10:c.20483C>G
(TTN)
|
ENSP00000352154.5:p.Thr6828Ser
|
|
ENST00000342175.10:c.20684C>G
(TTN)
|
ENSP00000340554.6:p.Thr6895Ser
|
|
ENST00000342992.10:c.39599C>G
(TTN)
|
ENSP00000343764.6:p.Thr13200Ser
|
|
ENST00000359218.9:c.20483C>G
(TTN)
|
ENSP00000352154.5:p.Thr6828Ser
|
|
ENST00000460472.6:c.20108C>G
(TTN)
|
ENSP00000434586.1:p.Thr6703Ser
|
|
ENST00000589042.5:c.47303C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr15768Ser
|
|
ENST00000591111.5:c.42380C>G
(TTN)
|
ENSP00000465570.1:p.Thr14127Ser
|
|
ENST00000615779.4:c.42380C>G
(TTN)
|
ENSP00000483597.1:p.Thr14127Ser
|
|
NM_001256850.1:c.42380C>G
(TTN)
|
NP_001243779.1:p.Thr14127Ser
|
|
NM_001267550.2:c.47303C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr15768Ser
|
|
NM_003319.4:c.20108C>G
(TTN)
|
NP_003310.4:p.Thr6703Ser
|
|
NM_133378.4:c.39599C>G
(TTN)
|
NP_596869.4:p.Thr13200Ser
|
|
NM_133432.3:c.20483C>G
(TTN)
|
NP_597676.3:p.Thr6828Ser
|
|
NM_133437.4:c.20684C>G
(TTN)
|
NP_597681.4:p.Thr6895Ser
|
|
NR_038271.1:n.1605-1705G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.46400C>G
(TTN)
|
XP_011510031.1:p.Thr15467Ser
|
|
XM_011511730.1:c.20294C>G
(TTN)
|
XP_011510032.1:p.Thr6765Ser
|
|
XM_011511731.1:c.20153C>G
(TTN)
|
XP_011510033.1:p.Thr6718Ser
|
|
XM_017004819.1:c.46196C>G
(TTN)
|
XP_016860308.1:p.Thr15399Ser
|
|
XM_017004820.1:c.41594C>G
(TTN)
|
XP_016860309.1:p.Thr13865Ser
|
|
XM_017004821.1:c.41591C>G
(TTN)
|
XP_016860310.1:p.Thr13864Ser
|
|
XM_017004822.1:c.38633C>G
(TTN)
|
XP_016860311.1:p.Thr12878Ser
|
|
XM_017004823.1:c.20249C>G
(TTN)
|
XP_016860312.1:p.Thr6750Ser
|
|
XM_024453094.1:c.41744C>G
(TTN)
|
XP_024308862.1:p.Thr13915Ser
|
|
XM_024453095.1:c.41741C>G
(TTN)
|
XP_024308863.1:p.Thr13914Ser
|
|
XM_024453096.1:c.41174C>G
(TTN)
|
XP_024308864.1:p.Thr13725Ser
|
|
XM_024453097.1:c.38516C>G
(TTN)
|
XP_024308865.1:p.Thr12839Ser
|
|
XM_024453098.1:c.38435C>G
(TTN)
|
XP_024308866.1:p.Thr12812Ser
|
|
XM_024453099.1:c.20198C>G
(TTN)
|
XP_024308867.1:p.Thr6733Ser
|
|
XM_024453100.1:c.10052C>G
(TTN)
|
XP_024308868.1:p.Thr3351Ser
|
|