ENST00000342992.11:c.86186A>C
(TTN)
|
ENSP00000343764.6:p.Lys28729Thr
|
|
ENST00000342175.11:c.67271A>C
(TTN)
|
ENSP00000340554.6:p.Lys22424Thr
|
|
ENST00000359218.10:c.67070A>C
(TTN)
|
ENSP00000352154.5:p.Lys22357Thr
|
|
ENST00000342175.10:c.67271A>C
(TTN)
|
ENSP00000340554.6:p.Lys22424Thr
|
|
ENST00000342992.10:c.86186A>C
(TTN)
|
ENSP00000343764.6:p.Lys28729Thr
|
|
ENST00000359218.9:c.67070A>C
(TTN)
|
ENSP00000352154.5:p.Lys22357Thr
|
|
ENST00000460472.6:c.66695A>C
(TTN)
|
ENSP00000434586.1:p.Lys22232Thr
|
|
ENST00000589042.5:c.93890A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Lys31297Thr
|
|
ENST00000591111.5:c.88967A>C
(TTN)
|
ENSP00000465570.1:p.Lys29656Thr
|
|
ENST00000615779.4:c.88967A>C
(TTN)
|
ENSP00000483597.1:p.Lys29656Thr
|
|
NM_001256850.1:c.88967A>C
(TTN)
|
NP_001243779.1:p.Lys29656Thr
|
|
NM_001267550.2:c.93890A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Lys31297Thr
|
|
NM_003319.4:c.66695A>C
(TTN)
|
NP_003310.4:p.Lys22232Thr
|
|
NM_133378.4:c.86186A>C
(TTN)
|
NP_596869.4:p.Lys28729Thr
|
|
NM_133432.3:c.67070A>C
(TTN)
|
NP_597676.3:p.Lys22357Thr
|
|
NM_133437.4:c.67271A>C
(TTN)
|
NP_597681.4:p.Lys22424Thr
|
|
NR_038271.1:n.447-23564T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+5375T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.92987A>C
(TTN)
|
XP_011510031.1:p.Lys30996Thr
|
|
XM_011511730.1:c.66881A>C
(TTN)
|
XP_011510032.1:p.Lys22294Thr
|
|
XM_011511731.1:c.66740A>C
(TTN)
|
XP_011510033.1:p.Lys22247Thr
|
|
XM_017004819.1:c.92783A>C
(TTN)
|
XP_016860308.1:p.Lys30928Thr
|
|
XM_017004820.1:c.88181A>C
(TTN)
|
XP_016860309.1:p.Lys29394Thr
|
|
XM_017004821.1:c.88178A>C
(TTN)
|
XP_016860310.1:p.Lys29393Thr
|
|
XM_017004822.1:c.85220A>C
(TTN)
|
XP_016860311.1:p.Lys28407Thr
|
|
XM_017004823.1:c.66836A>C
(TTN)
|
XP_016860312.1:p.Lys22279Thr
|
|
XM_024453094.1:c.88331A>C
(TTN)
|
XP_024308862.1:p.Lys29444Thr
|
|
XM_024453095.1:c.88328A>C
(TTN)
|
XP_024308863.1:p.Lys29443Thr
|
|
XM_024453096.1:c.87761A>C
(TTN)
|
XP_024308864.1:p.Lys29254Thr
|
|
XM_024453097.1:c.85103A>C
(TTN)
|
XP_024308865.1:p.Lys28368Thr
|
|
XM_024453098.1:c.85022A>C
(TTN)
|
XP_024308866.1:p.Lys28341Thr
|
|
XM_024453099.1:c.66785A>C
(TTN)
|
XP_024308867.1:p.Lys22262Thr
|
|
XM_024453100.1:c.56639A>C
(TTN)
|
XP_024308868.1:p.Lys18880Thr
|
|