ENST00000342992.11:c.98304T>G
(TTN)
|
ENSP00000343764.6:p.Tyr32768Ter
|
|
ENST00000342175.11:c.79389T>G
(TTN)
|
ENSP00000340554.6:p.Tyr26463Ter
|
|
ENST00000359218.10:c.79188T>G
(TTN)
|
ENSP00000352154.5:p.Tyr26396Ter
|
|
ENST00000342175.10:c.79389T>G
(TTN)
|
ENSP00000340554.6:p.Tyr26463Ter
|
|
ENST00000342992.10:c.98304T>G
(TTN)
|
ENSP00000343764.6:p.Tyr32768Ter
|
|
ENST00000359218.9:c.79188T>G
(TTN)
|
ENSP00000352154.5:p.Tyr26396Ter
|
|
ENST00000460472.6:c.78813T>G
(TTN)
|
ENSP00000434586.1:p.Tyr26271Ter
|
|
ENST00000589042.5:c.106008T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr35336Ter
|
|
ENST00000591111.5:c.101085T>G
(TTN)
|
ENSP00000465570.1:p.Tyr33695Ter
|
|
ENST00000615779.4:c.101085T>G
(TTN)
|
ENSP00000483597.1:p.Tyr33695Ter
|
|
NM_001256850.1:c.101085T>G
(TTN)
|
NP_001243779.1:p.Tyr33695Ter
|
|
NM_001267550.2:c.106008T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr35336Ter
|
|
NM_003319.4:c.78813T>G
(TTN)
|
NP_003310.4:p.Tyr26271Ter
|
|
NM_133378.4:c.98304T>G
(TTN)
|
NP_596869.4:p.Tyr32768Ter
|
|
NM_133432.3:c.79188T>G
(TTN)
|
NP_597676.3:p.Tyr26396Ter
|
|
NM_133437.4:c.79389T>G
(TTN)
|
NP_597681.4:p.Tyr26463Ter
|
|
NR_038271.1:n.446+6971A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5125A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105105T>G
(TTN)
|
XP_011510031.1:p.Tyr35035Ter
|
|
XM_011511730.1:c.78999T>G
(TTN)
|
XP_011510032.1:p.Tyr26333Ter
|
|
XM_011511731.1:c.78858T>G
(TTN)
|
XP_011510033.1:p.Tyr26286Ter
|
|
XM_017004819.1:c.104901T>G
(TTN)
|
XP_016860308.1:p.Tyr34967Ter
|
|
XM_017004820.1:c.100299T>G
(TTN)
|
XP_016860309.1:p.Tyr33433Ter
|
|
XM_017004821.1:c.100296T>G
(TTN)
|
XP_016860310.1:p.Tyr33432Ter
|
|
XM_017004822.1:c.97338T>G
(TTN)
|
XP_016860311.1:p.Tyr32446Ter
|
|
XM_017004823.1:c.78954T>G
(TTN)
|
XP_016860312.1:p.Tyr26318Ter
|
|
XM_024453094.1:c.100449T>G
(TTN)
|
XP_024308862.1:p.Tyr33483Ter
|
|
XM_024453095.1:c.100446T>G
(TTN)
|
XP_024308863.1:p.Tyr33482Ter
|
|
XM_024453096.1:c.99879T>G
(TTN)
|
XP_024308864.1:p.Tyr33293Ter
|
|
XM_024453097.1:c.97221T>G
(TTN)
|
XP_024308865.1:p.Tyr32407Ter
|
|
XM_024453098.1:c.97140T>G
(TTN)
|
XP_024308866.1:p.Tyr32380Ter
|
|
XM_024453099.1:c.78903T>G
(TTN)
|
XP_024308867.1:p.Tyr26301Ter
|
|
XM_024453100.1:c.68757T>G
(TTN)
|
XP_024308868.1:p.Tyr22919Ter
|
|