ENST00000342992.11:c.87411G>A
(TTN)
|
ENSP00000343764.6:p.Val29137=
|
|
ENST00000342175.11:c.68496G>A
(TTN)
|
ENSP00000340554.6:p.Val22832=
|
|
ENST00000359218.10:c.68295G>A
(TTN)
|
ENSP00000352154.5:p.Val22765=
|
|
ENST00000342175.10:c.68496G>A
(TTN)
|
ENSP00000340554.6:p.Val22832=
|
|
ENST00000342992.10:c.87411G>A
(TTN)
|
ENSP00000343764.6:p.Val29137=
|
|
ENST00000359218.9:c.68295G>A
(TTN)
|
ENSP00000352154.5:p.Val22765=
|
|
ENST00000460472.6:c.67920G>A
(TTN)
|
ENSP00000434586.1:p.Val22640=
|
|
ENST00000589042.5:c.95115G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val31705=
|
|
ENST00000591111.5:c.90192G>A
(TTN)
|
ENSP00000465570.1:p.Val30064=
|
|
ENST00000615779.4:c.90192G>A
(TTN)
|
ENSP00000483597.1:p.Val30064=
|
|
NM_001256850.1:c.90192G>A
(TTN)
|
NP_001243779.1:p.Val30064=
|
|
NM_001267550.2:c.95115G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Val31705=
|
|
NM_003319.4:c.67920G>A
(TTN)
|
NP_003310.4:p.Val22640=
|
|
NM_133378.4:c.87411G>A
(TTN)
|
NP_596869.4:p.Val29137=
|
|
NM_133432.3:c.68295G>A
(TTN)
|
NP_597676.3:p.Val22765=
|
|
NM_133437.4:c.68496G>A
(TTN)
|
NP_597681.4:p.Val22832=
|
|
NR_038271.1:n.446+22580C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+3855C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.94212G>A
(TTN)
|
XP_011510031.1:p.Val31404=
|
|
XM_011511730.1:c.68106G>A
(TTN)
|
XP_011510032.1:p.Val22702=
|
|
XM_011511731.1:c.67965G>A
(TTN)
|
XP_011510033.1:p.Val22655=
|
|
XM_017004819.1:c.94008G>A
(TTN)
|
XP_016860308.1:p.Val31336=
|
|
XM_017004820.1:c.89406G>A
(TTN)
|
XP_016860309.1:p.Val29802=
|
|
XM_017004821.1:c.89403G>A
(TTN)
|
XP_016860310.1:p.Val29801=
|
|
XM_017004822.1:c.86445G>A
(TTN)
|
XP_016860311.1:p.Val28815=
|
|
XM_017004823.1:c.68061G>A
(TTN)
|
XP_016860312.1:p.Val22687=
|
|
XM_024453094.1:c.89556G>A
(TTN)
|
XP_024308862.1:p.Val29852=
|
|
XM_024453095.1:c.89553G>A
(TTN)
|
XP_024308863.1:p.Val29851=
|
|
XM_024453096.1:c.88986G>A
(TTN)
|
XP_024308864.1:p.Val29662=
|
|
XM_024453097.1:c.86328G>A
(TTN)
|
XP_024308865.1:p.Val28776=
|
|
XM_024453098.1:c.86247G>A
(TTN)
|
XP_024308866.1:p.Val28749=
|
|
XM_024453099.1:c.68010G>A
(TTN)
|
XP_024308867.1:p.Val22670=
|
|
XM_024453100.1:c.57864G>A
(TTN)
|
XP_024308868.1:p.Val19288=
|
|