ENST00000342992.11:c.73913T>C
(TTN)
|
ENSP00000343764.6:p.Ile24638Thr
|
|
ENST00000342175.11:c.54998T>C
(TTN)
|
ENSP00000340554.6:p.Ile18333Thr
|
|
ENST00000359218.10:c.54797T>C
(TTN)
|
ENSP00000352154.5:p.Ile18266Thr
|
|
ENST00000342175.10:c.54998T>C
(TTN)
|
ENSP00000340554.6:p.Ile18333Thr
|
|
ENST00000342992.10:c.73913T>C
(TTN)
|
ENSP00000343764.6:p.Ile24638Thr
|
|
ENST00000359218.9:c.54797T>C
(TTN)
|
ENSP00000352154.5:p.Ile18266Thr
|
|
ENST00000460472.6:c.54422T>C
(TTN)
|
ENSP00000434586.1:p.Ile18141Thr
|
|
ENST00000589042.5:c.81617T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile27206Thr
|
|
ENST00000591111.5:c.76694T>C
(TTN)
|
ENSP00000465570.1:p.Ile25565Thr
|
|
ENST00000615779.4:c.76694T>C
(TTN)
|
ENSP00000483597.1:p.Ile25565Thr
|
|
NM_001256850.1:c.76694T>C
(TTN)
|
NP_001243779.1:p.Ile25565Thr
|
|
NM_001267550.2:c.81617T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ile27206Thr
|
|
NM_003319.4:c.54422T>C
(TTN)
|
NP_003310.4:p.Ile18141Thr
|
|
NM_133378.4:c.73913T>C
(TTN)
|
NP_596869.4:p.Ile24638Thr
|
|
NM_133432.3:c.54797T>C
(TTN)
|
NP_597676.3:p.Ile18266Thr
|
|
NM_133437.4:c.54998T>C
(TTN)
|
NP_597681.4:p.Ile18333Thr
|
|
NR_038271.1:n.447-6785A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-18057A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.80714T>C
(TTN)
|
XP_011510031.1:p.Ile26905Thr
|
|
XM_011511730.1:c.54608T>C
(TTN)
|
XP_011510032.1:p.Ile18203Thr
|
|
XM_011511731.1:c.54467T>C
(TTN)
|
XP_011510033.1:p.Ile18156Thr
|
|
XM_017004819.1:c.80510T>C
(TTN)
|
XP_016860308.1:p.Ile26837Thr
|
|
XM_017004820.1:c.75908T>C
(TTN)
|
XP_016860309.1:p.Ile25303Thr
|
|
XM_017004821.1:c.75905T>C
(TTN)
|
XP_016860310.1:p.Ile25302Thr
|
|
XM_017004822.1:c.72947T>C
(TTN)
|
XP_016860311.1:p.Ile24316Thr
|
|
XM_017004823.1:c.54563T>C
(TTN)
|
XP_016860312.1:p.Ile18188Thr
|
|
XM_024453094.1:c.76058T>C
(TTN)
|
XP_024308862.1:p.Ile25353Thr
|
|
XM_024453095.1:c.76055T>C
(TTN)
|
XP_024308863.1:p.Ile25352Thr
|
|
XM_024453096.1:c.75488T>C
(TTN)
|
XP_024308864.1:p.Ile25163Thr
|
|
XM_024453097.1:c.72830T>C
(TTN)
|
XP_024308865.1:p.Ile24277Thr
|
|
XM_024453098.1:c.72749T>C
(TTN)
|
XP_024308866.1:p.Ile24250Thr
|
|
XM_024453099.1:c.54512T>C
(TTN)
|
XP_024308867.1:p.Ile18171Thr
|
|
XM_024453100.1:c.44366T>C
(TTN)
|
XP_024308868.1:p.Ile14789Thr
|
|