ENST00000342992.11:c.39596T>G
(TTN)
|
ENSP00000343764.6:p.Ile13199Ser
|
|
ENST00000342175.11:c.20681T>G
(TTN)
|
ENSP00000340554.6:p.Ile6894Ser
|
|
ENST00000359218.10:c.20480T>G
(TTN)
|
ENSP00000352154.5:p.Ile6827Ser
|
|
ENST00000342175.10:c.20681T>G
(TTN)
|
ENSP00000340554.6:p.Ile6894Ser
|
|
ENST00000342992.10:c.39596T>G
(TTN)
|
ENSP00000343764.6:p.Ile13199Ser
|
|
ENST00000359218.9:c.20480T>G
(TTN)
|
ENSP00000352154.5:p.Ile6827Ser
|
|
ENST00000460472.6:c.20105T>G
(TTN)
|
ENSP00000434586.1:p.Ile6702Ser
|
|
ENST00000589042.5:c.47300T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile15767Ser
|
|
ENST00000591111.5:c.42377T>G
(TTN)
|
ENSP00000465570.1:p.Ile14126Ser
|
|
ENST00000615779.4:c.42377T>G
(TTN)
|
ENSP00000483597.1:p.Ile14126Ser
|
|
NM_001256850.1:c.42377T>G
(TTN)
|
NP_001243779.1:p.Ile14126Ser
|
|
NM_001267550.2:c.47300T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ile15767Ser
|
|
NM_003319.4:c.20105T>G
(TTN)
|
NP_003310.4:p.Ile6702Ser
|
|
NM_133378.4:c.39596T>G
(TTN)
|
NP_596869.4:p.Ile13199Ser
|
|
NM_133432.3:c.20480T>G
(TTN)
|
NP_597676.3:p.Ile6827Ser
|
|
NM_133437.4:c.20681T>G
(TTN)
|
NP_597681.4:p.Ile6894Ser
|
|
NR_038271.1:n.1605-1702A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.46397T>G
(TTN)
|
XP_011510031.1:p.Ile15466Ser
|
|
XM_011511730.1:c.20291T>G
(TTN)
|
XP_011510032.1:p.Ile6764Ser
|
|
XM_011511731.1:c.20150T>G
(TTN)
|
XP_011510033.1:p.Ile6717Ser
|
|
XM_017004819.1:c.46193T>G
(TTN)
|
XP_016860308.1:p.Ile15398Ser
|
|
XM_017004820.1:c.41591T>G
(TTN)
|
XP_016860309.1:p.Ile13864Ser
|
|
XM_017004821.1:c.41588T>G
(TTN)
|
XP_016860310.1:p.Ile13863Ser
|
|
XM_017004822.1:c.38630T>G
(TTN)
|
XP_016860311.1:p.Ile12877Ser
|
|
XM_017004823.1:c.20246T>G
(TTN)
|
XP_016860312.1:p.Ile6749Ser
|
|
XM_024453094.1:c.41741T>G
(TTN)
|
XP_024308862.1:p.Ile13914Ser
|
|
XM_024453095.1:c.41738T>G
(TTN)
|
XP_024308863.1:p.Ile13913Ser
|
|
XM_024453096.1:c.41171T>G
(TTN)
|
XP_024308864.1:p.Ile13724Ser
|
|
XM_024453097.1:c.38513T>G
(TTN)
|
XP_024308865.1:p.Ile12838Ser
|
|
XM_024453098.1:c.38432T>G
(TTN)
|
XP_024308866.1:p.Ile12811Ser
|
|
XM_024453099.1:c.20195T>G
(TTN)
|
XP_024308867.1:p.Ile6732Ser
|
|
XM_024453100.1:c.10049T>G
(TTN)
|
XP_024308868.1:p.Ile3350Ser
|
|