ENST00000342992.11:c.98454A>C
(TTN)
|
ENSP00000343764.6:p.Val32818=
|
|
ENST00000342175.11:c.79539A>C
(TTN)
|
ENSP00000340554.6:p.Val26513=
|
|
ENST00000359218.10:c.79338A>C
(TTN)
|
ENSP00000352154.5:p.Val26446=
|
|
ENST00000342175.10:c.79539A>C
(TTN)
|
ENSP00000340554.6:p.Val26513=
|
|
ENST00000342992.10:c.98454A>C
(TTN)
|
ENSP00000343764.6:p.Val32818=
|
|
ENST00000359218.9:c.79338A>C
(TTN)
|
ENSP00000352154.5:p.Val26446=
|
|
ENST00000460472.6:c.78963A>C
(TTN)
|
ENSP00000434586.1:p.Val26321=
|
|
ENST00000589042.5:c.106158A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val35386=
|
|
ENST00000591111.5:c.101235A>C
(TTN)
|
ENSP00000465570.1:p.Val33745=
|
|
ENST00000615779.4:c.101235A>C
(TTN)
|
ENSP00000483597.1:p.Val33745=
|
|
NM_001256850.1:c.101235A>C
(TTN)
|
NP_001243779.1:p.Val33745=
|
|
NM_001267550.2:c.106158A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Val35386=
|
|
NM_003319.4:c.78963A>C
(TTN)
|
NP_003310.4:p.Val26321=
|
|
NM_133378.4:c.98454A>C
(TTN)
|
NP_596869.4:p.Val32818=
|
|
NM_133432.3:c.79338A>C
(TTN)
|
NP_597676.3:p.Val26446=
|
|
NM_133437.4:c.79539A>C
(TTN)
|
NP_597681.4:p.Val26513=
|
|
NR_038271.1:n.446+6821T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5275T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105255A>C
(TTN)
|
XP_011510031.1:p.Val35085=
|
|
XM_011511730.1:c.79149A>C
(TTN)
|
XP_011510032.1:p.Val26383=
|
|
XM_011511731.1:c.79008A>C
(TTN)
|
XP_011510033.1:p.Val26336=
|
|
XM_017004819.1:c.105051A>C
(TTN)
|
XP_016860308.1:p.Val35017=
|
|
XM_017004820.1:c.100449A>C
(TTN)
|
XP_016860309.1:p.Val33483=
|
|
XM_017004821.1:c.100446A>C
(TTN)
|
XP_016860310.1:p.Val33482=
|
|
XM_017004822.1:c.97488A>C
(TTN)
|
XP_016860311.1:p.Val32496=
|
|
XM_017004823.1:c.79104A>C
(TTN)
|
XP_016860312.1:p.Val26368=
|
|
XM_024453094.1:c.100599A>C
(TTN)
|
XP_024308862.1:p.Val33533=
|
|
XM_024453095.1:c.100596A>C
(TTN)
|
XP_024308863.1:p.Val33532=
|
|
XM_024453096.1:c.100029A>C
(TTN)
|
XP_024308864.1:p.Val33343=
|
|
XM_024453097.1:c.97371A>C
(TTN)
|
XP_024308865.1:p.Val32457=
|
|
XM_024453098.1:c.97290A>C
(TTN)
|
XP_024308866.1:p.Val32430=
|
|
XM_024453099.1:c.79053A>C
(TTN)
|
XP_024308867.1:p.Val26351=
|
|
XM_024453100.1:c.68907A>C
(TTN)
|
XP_024308868.1:p.Val22969=
|
|