ENST00000342992.11:c.39595A>G
(TTN)
|
ENSP00000343764.6:p.Ile13199Val
|
|
ENST00000342175.11:c.20680A>G
(TTN)
|
ENSP00000340554.6:p.Ile6894Val
|
|
ENST00000359218.10:c.20479A>G
(TTN)
|
ENSP00000352154.5:p.Ile6827Val
|
|
ENST00000342175.10:c.20680A>G
(TTN)
|
ENSP00000340554.6:p.Ile6894Val
|
|
ENST00000342992.10:c.39595A>G
(TTN)
|
ENSP00000343764.6:p.Ile13199Val
|
|
ENST00000359218.9:c.20479A>G
(TTN)
|
ENSP00000352154.5:p.Ile6827Val
|
|
ENST00000460472.6:c.20104A>G
(TTN)
|
ENSP00000434586.1:p.Ile6702Val
|
|
ENST00000589042.5:c.47299A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile15767Val
|
|
ENST00000591111.5:c.42376A>G
(TTN)
|
ENSP00000465570.1:p.Ile14126Val
|
|
ENST00000615779.4:c.42376A>G
(TTN)
|
ENSP00000483597.1:p.Ile14126Val
|
|
NM_001256850.1:c.42376A>G
(TTN)
|
NP_001243779.1:p.Ile14126Val
|
|
NM_001267550.2:c.47299A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ile15767Val
|
|
NM_003319.4:c.20104A>G
(TTN)
|
NP_003310.4:p.Ile6702Val
|
|
NM_133378.4:c.39595A>G
(TTN)
|
NP_596869.4:p.Ile13199Val
|
|
NM_133432.3:c.20479A>G
(TTN)
|
NP_597676.3:p.Ile6827Val
|
|
NM_133437.4:c.20680A>G
(TTN)
|
NP_597681.4:p.Ile6894Val
|
|
NR_038271.1:n.1605-1701T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.46396A>G
(TTN)
|
XP_011510031.1:p.Ile15466Val
|
|
XM_011511730.1:c.20290A>G
(TTN)
|
XP_011510032.1:p.Ile6764Val
|
|
XM_011511731.1:c.20149A>G
(TTN)
|
XP_011510033.1:p.Ile6717Val
|
|
XM_017004819.1:c.46192A>G
(TTN)
|
XP_016860308.1:p.Ile15398Val
|
|
XM_017004820.1:c.41590A>G
(TTN)
|
XP_016860309.1:p.Ile13864Val
|
|
XM_017004821.1:c.41587A>G
(TTN)
|
XP_016860310.1:p.Ile13863Val
|
|
XM_017004822.1:c.38629A>G
(TTN)
|
XP_016860311.1:p.Ile12877Val
|
|
XM_017004823.1:c.20245A>G
(TTN)
|
XP_016860312.1:p.Ile6749Val
|
|
XM_024453094.1:c.41740A>G
(TTN)
|
XP_024308862.1:p.Ile13914Val
|
|
XM_024453095.1:c.41737A>G
(TTN)
|
XP_024308863.1:p.Ile13913Val
|
|
XM_024453096.1:c.41170A>G
(TTN)
|
XP_024308864.1:p.Ile13724Val
|
|
XM_024453097.1:c.38512A>G
(TTN)
|
XP_024308865.1:p.Ile12838Val
|
|
XM_024453098.1:c.38431A>G
(TTN)
|
XP_024308866.1:p.Ile12811Val
|
|
XM_024453099.1:c.20194A>G
(TTN)
|
XP_024308867.1:p.Ile6732Val
|
|
XM_024453100.1:c.10048A>G
(TTN)
|
XP_024308868.1:p.Ile3350Val
|
|