ENST00000342992.11:c.98725T>C
(TTN)
|
ENSP00000343764.6:p.Leu32909=
|
|
ENST00000342175.11:c.79810T>C
(TTN)
|
ENSP00000340554.6:p.Leu26604=
|
|
ENST00000359218.10:c.79609T>C
(TTN)
|
ENSP00000352154.5:p.Leu26537=
|
|
ENST00000342175.10:c.79810T>C
(TTN)
|
ENSP00000340554.6:p.Leu26604=
|
|
ENST00000342992.10:c.98725T>C
(TTN)
|
ENSP00000343764.6:p.Leu32909=
|
|
ENST00000359218.9:c.79609T>C
(TTN)
|
ENSP00000352154.5:p.Leu26537=
|
|
ENST00000460472.6:c.79234T>C
(TTN)
|
ENSP00000434586.1:p.Leu26412=
|
|
ENST00000589042.5:c.106429T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu35477=
|
|
ENST00000591111.5:c.101506T>C
(TTN)
|
ENSP00000465570.1:p.Leu33836=
|
|
ENST00000615779.4:c.101506T>C
(TTN)
|
ENSP00000483597.1:p.Leu33836=
|
|
NM_001256850.1:c.101506T>C
(TTN)
|
NP_001243779.1:p.Leu33836=
|
|
NM_001267550.2:c.106429T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Leu35477=
|
|
NM_003319.4:c.79234T>C
(TTN)
|
NP_003310.4:p.Leu26412=
|
|
NM_133378.4:c.98725T>C
(TTN)
|
NP_596869.4:p.Leu32909=
|
|
NM_133432.3:c.79609T>C
(TTN)
|
NP_597676.3:p.Leu26537=
|
|
NM_133437.4:c.79810T>C
(TTN)
|
NP_597681.4:p.Leu26604=
|
|
NR_038271.1:n.446+6426A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5670A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105526T>C
(TTN)
|
XP_011510031.1:p.Leu35176=
|
|
XM_011511730.1:c.79420T>C
(TTN)
|
XP_011510032.1:p.Leu26474=
|
|
XM_011511731.1:c.79279T>C
(TTN)
|
XP_011510033.1:p.Leu26427=
|
|
XM_017004819.1:c.105322T>C
(TTN)
|
XP_016860308.1:p.Leu35108=
|
|
XM_017004820.1:c.100720T>C
(TTN)
|
XP_016860309.1:p.Leu33574=
|
|
XM_017004821.1:c.100717T>C
(TTN)
|
XP_016860310.1:p.Leu33573=
|
|
XM_017004822.1:c.97759T>C
(TTN)
|
XP_016860311.1:p.Leu32587=
|
|
XM_017004823.1:c.79375T>C
(TTN)
|
XP_016860312.1:p.Leu26459=
|
|
XM_024453094.1:c.100870T>C
(TTN)
|
XP_024308862.1:p.Leu33624=
|
|
XM_024453095.1:c.100867T>C
(TTN)
|
XP_024308863.1:p.Leu33623=
|
|
XM_024453096.1:c.100300T>C
(TTN)
|
XP_024308864.1:p.Leu33434=
|
|
XM_024453097.1:c.97642T>C
(TTN)
|
XP_024308865.1:p.Leu32548=
|
|
XM_024453098.1:c.97561T>C
(TTN)
|
XP_024308866.1:p.Leu32521=
|
|
XM_024453099.1:c.79324T>C
(TTN)
|
XP_024308867.1:p.Leu26442=
|
|
XM_024453100.1:c.69178T>C
(TTN)
|
XP_024308868.1:p.Leu23060=
|
|