ENST00000342992.11:c.51349G>T
(TTN)
|
ENSP00000343764.6:p.Val17117Phe
|
|
ENST00000342175.11:c.32434G>T
(TTN)
|
ENSP00000340554.6:p.Val10812Phe
|
|
ENST00000359218.10:c.32233G>T
(TTN)
|
ENSP00000352154.5:p.Val10745Phe
|
|
ENST00000342175.10:c.32434G>T
(TTN)
|
ENSP00000340554.6:p.Val10812Phe
|
|
ENST00000342992.10:c.51349G>T
(TTN)
|
ENSP00000343764.6:p.Val17117Phe
|
|
ENST00000359218.9:c.32233G>T
(TTN)
|
ENSP00000352154.5:p.Val10745Phe
|
|
ENST00000460472.6:c.31858G>T
(TTN)
|
ENSP00000434586.1:p.Val10620Phe
|
|
ENST00000589042.5:c.59053G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val19685Phe
|
|
ENST00000591111.5:c.54130G>T
(TTN)
|
ENSP00000465570.1:p.Val18044Phe
|
|
ENST00000615779.4:c.54130G>T
(TTN)
|
ENSP00000483597.1:p.Val18044Phe
|
|
NM_001256850.1:c.54130G>T
(TTN)
|
NP_001243779.1:p.Val18044Phe
|
|
NM_001267550.2:c.59053G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Val19685Phe
|
|
NM_003319.4:c.31858G>T
(TTN)
|
NP_003310.4:p.Val10620Phe
|
|
NM_133378.4:c.51349G>T
(TTN)
|
NP_596869.4:p.Val17117Phe
|
|
NM_133432.3:c.32233G>T
(TTN)
|
NP_597676.3:p.Val10745Phe
|
|
NM_133437.4:c.32434G>T
(TTN)
|
NP_597681.4:p.Val10812Phe
|
|
NR_038271.1:n.597-4530C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1752C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.58150G>T
(TTN)
|
XP_011510031.1:p.Val19384Phe
|
|
XM_011511730.1:c.32044G>T
(TTN)
|
XP_011510032.1:p.Val10682Phe
|
|
XM_011511731.1:c.31903G>T
(TTN)
|
XP_011510033.1:p.Val10635Phe
|
|
XM_017004819.1:c.57946G>T
(TTN)
|
XP_016860308.1:p.Val19316Phe
|
|
XM_017004820.1:c.53344G>T
(TTN)
|
XP_016860309.1:p.Val17782Phe
|
|
XM_017004821.1:c.53341G>T
(TTN)
|
XP_016860310.1:p.Val17781Phe
|
|
XM_017004822.1:c.50383G>T
(TTN)
|
XP_016860311.1:p.Val16795Phe
|
|
XM_017004823.1:c.31999G>T
(TTN)
|
XP_016860312.1:p.Val10667Phe
|
|
XM_024453094.1:c.53494G>T
(TTN)
|
XP_024308862.1:p.Val17832Phe
|
|
XM_024453095.1:c.53491G>T
(TTN)
|
XP_024308863.1:p.Val17831Phe
|
|
XM_024453096.1:c.52924G>T
(TTN)
|
XP_024308864.1:p.Val17642Phe
|
|
XM_024453097.1:c.50266G>T
(TTN)
|
XP_024308865.1:p.Val16756Phe
|
|
XM_024453098.1:c.50185G>T
(TTN)
|
XP_024308866.1:p.Val16729Phe
|
|
XM_024453099.1:c.31948G>T
(TTN)
|
XP_024308867.1:p.Val10650Phe
|
|
XM_024453100.1:c.21802G>T
(TTN)
|
XP_024308868.1:p.Val7268Phe
|
|