ENST00000342992.11:c.98736T>C
(TTN)
|
ENSP00000343764.6:p.His32912=
|
|
ENST00000342175.11:c.79821T>C
(TTN)
|
ENSP00000340554.6:p.His26607=
|
|
ENST00000359218.10:c.79620T>C
(TTN)
|
ENSP00000352154.5:p.His26540=
|
|
ENST00000342175.10:c.79821T>C
(TTN)
|
ENSP00000340554.6:p.His26607=
|
|
ENST00000342992.10:c.98736T>C
(TTN)
|
ENSP00000343764.6:p.His32912=
|
|
ENST00000359218.9:c.79620T>C
(TTN)
|
ENSP00000352154.5:p.His26540=
|
|
ENST00000460472.6:c.79245T>C
(TTN)
|
ENSP00000434586.1:p.His26415=
|
|
ENST00000589042.5:c.106440T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.His35480=
|
|
ENST00000591111.5:c.101517T>C
(TTN)
|
ENSP00000465570.1:p.His33839=
|
|
ENST00000615779.4:c.101517T>C
(TTN)
|
ENSP00000483597.1:p.His33839=
|
|
NM_001256850.1:c.101517T>C
(TTN)
|
NP_001243779.1:p.His33839=
|
|
NM_001267550.2:c.106440T>C
(TTN)
MANE Select
|
NP_001254479.2:p.His35480=
|
|
NM_003319.4:c.79245T>C
(TTN)
|
NP_003310.4:p.His26415=
|
|
NM_133378.4:c.98736T>C
(TTN)
|
NP_596869.4:p.His32912=
|
|
NM_133432.3:c.79620T>C
(TTN)
|
NP_597676.3:p.His26540=
|
|
NM_133437.4:c.79821T>C
(TTN)
|
NP_597681.4:p.His26607=
|
|
NR_038271.1:n.446+6415A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5681A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105537T>C
(TTN)
|
XP_011510031.1:p.His35179=
|
|
XM_011511730.1:c.79431T>C
(TTN)
|
XP_011510032.1:p.His26477=
|
|
XM_011511731.1:c.79290T>C
(TTN)
|
XP_011510033.1:p.His26430=
|
|
XM_017004819.1:c.105333T>C
(TTN)
|
XP_016860308.1:p.His35111=
|
|
XM_017004820.1:c.100731T>C
(TTN)
|
XP_016860309.1:p.His33577=
|
|
XM_017004821.1:c.100728T>C
(TTN)
|
XP_016860310.1:p.His33576=
|
|
XM_017004822.1:c.97770T>C
(TTN)
|
XP_016860311.1:p.His32590=
|
|
XM_017004823.1:c.79386T>C
(TTN)
|
XP_016860312.1:p.His26462=
|
|
XM_024453094.1:c.100881T>C
(TTN)
|
XP_024308862.1:p.His33627=
|
|
XM_024453095.1:c.100878T>C
(TTN)
|
XP_024308863.1:p.His33626=
|
|
XM_024453096.1:c.100311T>C
(TTN)
|
XP_024308864.1:p.His33437=
|
|
XM_024453097.1:c.97653T>C
(TTN)
|
XP_024308865.1:p.His32551=
|
|
XM_024453098.1:c.97572T>C
(TTN)
|
XP_024308866.1:p.His32524=
|
|
XM_024453099.1:c.79335T>C
(TTN)
|
XP_024308867.1:p.His26445=
|
|
XM_024453100.1:c.69189T>C
(TTN)
|
XP_024308868.1:p.His23063=
|
|