ENST00000342992.11:c.88322T>C
(TTN)
|
ENSP00000343764.6:p.Ile29441Thr
|
|
ENST00000342175.11:c.69407T>C
(TTN)
|
ENSP00000340554.6:p.Ile23136Thr
|
|
ENST00000359218.10:c.69206T>C
(TTN)
|
ENSP00000352154.5:p.Ile23069Thr
|
|
ENST00000342175.10:c.69407T>C
(TTN)
|
ENSP00000340554.6:p.Ile23136Thr
|
|
ENST00000342992.10:c.88322T>C
(TTN)
|
ENSP00000343764.6:p.Ile29441Thr
|
|
ENST00000359218.9:c.69206T>C
(TTN)
|
ENSP00000352154.5:p.Ile23069Thr
|
|
ENST00000460472.6:c.68831T>C
(TTN)
|
ENSP00000434586.1:p.Ile22944Thr
|
|
ENST00000589042.5:c.96026T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile32009Thr
|
|
ENST00000591111.5:c.91103T>C
(TTN)
|
ENSP00000465570.1:p.Ile30368Thr
|
|
ENST00000615779.4:c.91103T>C
(TTN)
|
ENSP00000483597.1:p.Ile30368Thr
|
|
NM_001256850.1:c.91103T>C
(TTN)
|
NP_001243779.1:p.Ile30368Thr
|
|
NM_001267550.2:c.96026T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ile32009Thr
|
|
NM_003319.4:c.68831T>C
(TTN)
|
NP_003310.4:p.Ile22944Thr
|
|
NM_133378.4:c.88322T>C
(TTN)
|
NP_596869.4:p.Ile29441Thr
|
|
NM_133432.3:c.69206T>C
(TTN)
|
NP_597676.3:p.Ile23069Thr
|
|
NM_133437.4:c.69407T>C
(TTN)
|
NP_597681.4:p.Ile23136Thr
|
|
NR_038271.1:n.446+20567A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1842A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.95123T>C
(TTN)
|
XP_011510031.1:p.Ile31708Thr
|
|
XM_011511730.1:c.69017T>C
(TTN)
|
XP_011510032.1:p.Ile23006Thr
|
|
XM_011511731.1:c.68876T>C
(TTN)
|
XP_011510033.1:p.Ile22959Thr
|
|
XM_017004819.1:c.94919T>C
(TTN)
|
XP_016860308.1:p.Ile31640Thr
|
|
XM_017004820.1:c.90317T>C
(TTN)
|
XP_016860309.1:p.Ile30106Thr
|
|
XM_017004821.1:c.90314T>C
(TTN)
|
XP_016860310.1:p.Ile30105Thr
|
|
XM_017004822.1:c.87356T>C
(TTN)
|
XP_016860311.1:p.Ile29119Thr
|
|
XM_017004823.1:c.68972T>C
(TTN)
|
XP_016860312.1:p.Ile22991Thr
|
|
XM_024453094.1:c.90467T>C
(TTN)
|
XP_024308862.1:p.Ile30156Thr
|
|
XM_024453095.1:c.90464T>C
(TTN)
|
XP_024308863.1:p.Ile30155Thr
|
|
XM_024453096.1:c.89897T>C
(TTN)
|
XP_024308864.1:p.Ile29966Thr
|
|
XM_024453097.1:c.87239T>C
(TTN)
|
XP_024308865.1:p.Ile29080Thr
|
|
XM_024453098.1:c.87158T>C
(TTN)
|
XP_024308866.1:p.Ile29053Thr
|
|
XM_024453099.1:c.68921T>C
(TTN)
|
XP_024308867.1:p.Ile22974Thr
|
|
XM_024453100.1:c.58775T>C
(TTN)
|
XP_024308868.1:p.Ile19592Thr
|
|