ENST00000342992.11:c.96790T>A
(TTN)
|
ENSP00000343764.6:p.Ser32264Thr
|
|
ENST00000342175.11:c.77875T>A
(TTN)
|
ENSP00000340554.6:p.Ser25959Thr
|
|
ENST00000359218.10:c.77674T>A
(TTN)
|
ENSP00000352154.5:p.Ser25892Thr
|
|
ENST00000342175.10:c.77875T>A
(TTN)
|
ENSP00000340554.6:p.Ser25959Thr
|
|
ENST00000342992.10:c.96790T>A
(TTN)
|
ENSP00000343764.6:p.Ser32264Thr
|
|
ENST00000359218.9:c.77674T>A
(TTN)
|
ENSP00000352154.5:p.Ser25892Thr
|
|
ENST00000460472.6:c.77299T>A
(TTN)
|
ENSP00000434586.1:p.Ser25767Thr
|
|
ENST00000589042.5:c.104494T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34832Thr
|
|
ENST00000591111.5:c.99571T>A
(TTN)
|
ENSP00000465570.1:p.Ser33191Thr
|
|
ENST00000615779.4:c.99571T>A
(TTN)
|
ENSP00000483597.1:p.Ser33191Thr
|
|
NM_001256850.1:c.99571T>A
(TTN)
|
NP_001243779.1:p.Ser33191Thr
|
|
NM_001267550.2:c.104494T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34832Thr
|
|
NM_003319.4:c.77299T>A
(TTN)
|
NP_003310.4:p.Ser25767Thr
|
|
NM_133378.4:c.96790T>A
(TTN)
|
NP_596869.4:p.Ser32264Thr
|
|
NM_133432.3:c.77674T>A
(TTN)
|
NP_597676.3:p.Ser25892Thr
|
|
NM_133437.4:c.77875T>A
(TTN)
|
NP_597681.4:p.Ser25959Thr
|
|
NR_038271.1:n.446+8485A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3611A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.103591T>A
(TTN)
|
XP_011510031.1:p.Ser34531Thr
|
|
XM_011511730.1:c.77485T>A
(TTN)
|
XP_011510032.1:p.Ser25829Thr
|
|
XM_011511731.1:c.77344T>A
(TTN)
|
XP_011510033.1:p.Ser25782Thr
|
|
XM_017004819.1:c.103387T>A
(TTN)
|
XP_016860308.1:p.Ser34463Thr
|
|
XM_017004820.1:c.98785T>A
(TTN)
|
XP_016860309.1:p.Ser32929Thr
|
|
XM_017004821.1:c.98782T>A
(TTN)
|
XP_016860310.1:p.Ser32928Thr
|
|
XM_017004822.1:c.95824T>A
(TTN)
|
XP_016860311.1:p.Ser31942Thr
|
|
XM_017004823.1:c.77440T>A
(TTN)
|
XP_016860312.1:p.Ser25814Thr
|
|
XM_024453094.1:c.98935T>A
(TTN)
|
XP_024308862.1:p.Ser32979Thr
|
|
XM_024453095.1:c.98932T>A
(TTN)
|
XP_024308863.1:p.Ser32978Thr
|
|
XM_024453096.1:c.98365T>A
(TTN)
|
XP_024308864.1:p.Ser32789Thr
|
|
XM_024453097.1:c.95707T>A
(TTN)
|
XP_024308865.1:p.Ser31903Thr
|
|
XM_024453098.1:c.95626T>A
(TTN)
|
XP_024308866.1:p.Ser31876Thr
|
|
XM_024453099.1:c.77389T>A
(TTN)
|
XP_024308867.1:p.Ser25797Thr
|
|
XM_024453100.1:c.67243T>A
(TTN)
|
XP_024308868.1:p.Ser22415Thr
|
|