ENST00000342992.11:c.72161C>A
(TTN)
|
ENSP00000343764.6:p.Pro24054His
|
|
ENST00000342175.11:c.53246C>A
(TTN)
|
ENSP00000340554.6:p.Pro17749His
|
|
ENST00000359218.10:c.53045C>A
(TTN)
|
ENSP00000352154.5:p.Pro17682His
|
|
ENST00000342175.10:c.53246C>A
(TTN)
|
ENSP00000340554.6:p.Pro17749His
|
|
ENST00000342992.10:c.72161C>A
(TTN)
|
ENSP00000343764.6:p.Pro24054His
|
|
ENST00000359218.9:c.53045C>A
(TTN)
|
ENSP00000352154.5:p.Pro17682His
|
|
ENST00000460472.6:c.52670C>A
(TTN)
|
ENSP00000434586.1:p.Pro17557His
|
|
ENST00000589042.5:c.79865C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro26622His
|
|
ENST00000591111.5:c.74942C>A
(TTN)
|
ENSP00000465570.1:p.Pro24981His
|
|
ENST00000615779.4:c.74942C>A
(TTN)
|
ENSP00000483597.1:p.Pro24981His
|
|
NM_001256850.1:c.74942C>A
(TTN)
|
NP_001243779.1:p.Pro24981His
|
|
NM_001267550.2:c.79865C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Pro26622His
|
|
NM_003319.4:c.52670C>A
(TTN)
|
NP_003310.4:p.Pro17557His
|
|
NM_133378.4:c.72161C>A
(TTN)
|
NP_596869.4:p.Pro24054His
|
|
NM_133432.3:c.53045C>A
(TTN)
|
NP_597676.3:p.Pro17682His
|
|
NM_133437.4:c.53246C>A
(TTN)
|
NP_597681.4:p.Pro17749His
|
|
NR_038271.1:n.447-5033G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-16305G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.78962C>A
(TTN)
|
XP_011510031.1:p.Pro26321His
|
|
XM_011511730.1:c.52856C>A
(TTN)
|
XP_011510032.1:p.Pro17619His
|
|
XM_011511731.1:c.52715C>A
(TTN)
|
XP_011510033.1:p.Pro17572His
|
|
XM_017004819.1:c.78758C>A
(TTN)
|
XP_016860308.1:p.Pro26253His
|
|
XM_017004820.1:c.74156C>A
(TTN)
|
XP_016860309.1:p.Pro24719His
|
|
XM_017004821.1:c.74153C>A
(TTN)
|
XP_016860310.1:p.Pro24718His
|
|
XM_017004822.1:c.71195C>A
(TTN)
|
XP_016860311.1:p.Pro23732His
|
|
XM_017004823.1:c.52811C>A
(TTN)
|
XP_016860312.1:p.Pro17604His
|
|
XM_024453094.1:c.74306C>A
(TTN)
|
XP_024308862.1:p.Pro24769His
|
|
XM_024453095.1:c.74303C>A
(TTN)
|
XP_024308863.1:p.Pro24768His
|
|
XM_024453096.1:c.73736C>A
(TTN)
|
XP_024308864.1:p.Pro24579His
|
|
XM_024453097.1:c.71078C>A
(TTN)
|
XP_024308865.1:p.Pro23693His
|
|
XM_024453098.1:c.70997C>A
(TTN)
|
XP_024308866.1:p.Pro23666His
|
|
XM_024453099.1:c.52760C>A
(TTN)
|
XP_024308867.1:p.Pro17587His
|
|
XM_024453100.1:c.42614C>A
(TTN)
|
XP_024308868.1:p.Pro14205His
|
|