ENST00000342992.11:c.98438G>C
(TTN)
|
ENSP00000343764.6:p.Ser32813Thr
|
|
ENST00000342175.11:c.79523G>C
(TTN)
|
ENSP00000340554.6:p.Ser26508Thr
|
|
ENST00000359218.10:c.79322G>C
(TTN)
|
ENSP00000352154.5:p.Ser26441Thr
|
|
ENST00000342175.10:c.79523G>C
(TTN)
|
ENSP00000340554.6:p.Ser26508Thr
|
|
ENST00000342992.10:c.98438G>C
(TTN)
|
ENSP00000343764.6:p.Ser32813Thr
|
|
ENST00000359218.9:c.79322G>C
(TTN)
|
ENSP00000352154.5:p.Ser26441Thr
|
|
ENST00000460472.6:c.78947G>C
(TTN)
|
ENSP00000434586.1:p.Ser26316Thr
|
|
ENST00000589042.5:c.106142G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser35381Thr
|
|
ENST00000591111.5:c.101219G>C
(TTN)
|
ENSP00000465570.1:p.Ser33740Thr
|
|
ENST00000615779.4:c.101219G>C
(TTN)
|
ENSP00000483597.1:p.Ser33740Thr
|
|
NM_001256850.1:c.101219G>C
(TTN)
|
NP_001243779.1:p.Ser33740Thr
|
|
NM_001267550.2:c.106142G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ser35381Thr
|
|
NM_003319.4:c.78947G>C
(TTN)
|
NP_003310.4:p.Ser26316Thr
|
|
NM_133378.4:c.98438G>C
(TTN)
|
NP_596869.4:p.Ser32813Thr
|
|
NM_133432.3:c.79322G>C
(TTN)
|
NP_597676.3:p.Ser26441Thr
|
|
NM_133437.4:c.79523G>C
(TTN)
|
NP_597681.4:p.Ser26508Thr
|
|
NR_038271.1:n.446+6837C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5259C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105239G>C
(TTN)
|
XP_011510031.1:p.Ser35080Thr
|
|
XM_011511730.1:c.79133G>C
(TTN)
|
XP_011510032.1:p.Ser26378Thr
|
|
XM_011511731.1:c.78992G>C
(TTN)
|
XP_011510033.1:p.Ser26331Thr
|
|
XM_017004819.1:c.105035G>C
(TTN)
|
XP_016860308.1:p.Ser35012Thr
|
|
XM_017004820.1:c.100433G>C
(TTN)
|
XP_016860309.1:p.Ser33478Thr
|
|
XM_017004821.1:c.100430G>C
(TTN)
|
XP_016860310.1:p.Ser33477Thr
|
|
XM_017004822.1:c.97472G>C
(TTN)
|
XP_016860311.1:p.Ser32491Thr
|
|
XM_017004823.1:c.79088G>C
(TTN)
|
XP_016860312.1:p.Ser26363Thr
|
|
XM_024453094.1:c.100583G>C
(TTN)
|
XP_024308862.1:p.Ser33528Thr
|
|
XM_024453095.1:c.100580G>C
(TTN)
|
XP_024308863.1:p.Ser33527Thr
|
|
XM_024453096.1:c.100013G>C
(TTN)
|
XP_024308864.1:p.Ser33338Thr
|
|
XM_024453097.1:c.97355G>C
(TTN)
|
XP_024308865.1:p.Ser32452Thr
|
|
XM_024453098.1:c.97274G>C
(TTN)
|
XP_024308866.1:p.Ser32425Thr
|
|
XM_024453099.1:c.79037G>C
(TTN)
|
XP_024308867.1:p.Ser26346Thr
|
|
XM_024453100.1:c.68891G>C
(TTN)
|
XP_024308868.1:p.Ser22964Thr
|
|