ENST00000342992.11:c.39062T>C
(TTN)
|
ENSP00000343764.6:p.Val13021Ala
|
|
ENST00000342175.11:c.20147T>C
(TTN)
|
ENSP00000340554.6:p.Val6716Ala
|
|
ENST00000359218.10:c.19946T>C
(TTN)
|
ENSP00000352154.5:p.Val6649Ala
|
|
ENST00000342175.10:c.20147T>C
(TTN)
|
ENSP00000340554.6:p.Val6716Ala
|
|
ENST00000342992.10:c.39062T>C
(TTN)
|
ENSP00000343764.6:p.Val13021Ala
|
|
ENST00000359218.9:c.19946T>C
(TTN)
|
ENSP00000352154.5:p.Val6649Ala
|
|
ENST00000460472.6:c.19571T>C
(TTN)
|
ENSP00000434586.1:p.Val6524Ala
|
|
ENST00000589042.5:c.46766T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val15589Ala
|
|
ENST00000591111.5:c.41843T>C
(TTN)
|
ENSP00000465570.1:p.Val13948Ala
|
|
ENST00000615779.4:c.41843T>C
(TTN)
|
ENSP00000483597.1:p.Val13948Ala
|
|
NM_001256850.1:c.41843T>C
(TTN)
|
NP_001243779.1:p.Val13948Ala
|
|
NM_001267550.2:c.46766T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Val15589Ala
|
|
NM_003319.4:c.19571T>C
(TTN)
|
NP_003310.4:p.Val6524Ala
|
|
NM_133378.4:c.39062T>C
(TTN)
|
NP_596869.4:p.Val13021Ala
|
|
NM_133432.3:c.19946T>C
(TTN)
|
NP_597676.3:p.Val6649Ala
|
|
NM_133437.4:c.20147T>C
(TTN)
|
NP_597681.4:p.Val6716Ala
|
|
NR_038271.1:n.1605-969A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.45863T>C
(TTN)
|
XP_011510031.1:p.Val15288Ala
|
|
XM_011511730.1:c.19757T>C
(TTN)
|
XP_011510032.1:p.Val6586Ala
|
|
XM_011511731.1:c.19616T>C
(TTN)
|
XP_011510033.1:p.Val6539Ala
|
|
XM_017004819.1:c.45659T>C
(TTN)
|
XP_016860308.1:p.Val15220Ala
|
|
XM_017004820.1:c.41057T>C
(TTN)
|
XP_016860309.1:p.Val13686Ala
|
|
XM_017004821.1:c.41054T>C
(TTN)
|
XP_016860310.1:p.Val13685Ala
|
|
XM_017004822.1:c.38096T>C
(TTN)
|
XP_016860311.1:p.Val12699Ala
|
|
XM_017004823.1:c.19712T>C
(TTN)
|
XP_016860312.1:p.Val6571Ala
|
|
XM_024453094.1:c.41207T>C
(TTN)
|
XP_024308862.1:p.Val13736Ala
|
|
XM_024453095.1:c.41204T>C
(TTN)
|
XP_024308863.1:p.Val13735Ala
|
|
XM_024453096.1:c.40637T>C
(TTN)
|
XP_024308864.1:p.Val13546Ala
|
|
XM_024453097.1:c.37979T>C
(TTN)
|
XP_024308865.1:p.Val12660Ala
|
|
XM_024453098.1:c.37898T>C
(TTN)
|
XP_024308866.1:p.Val12633Ala
|
|
XM_024453099.1:c.19661T>C
(TTN)
|
XP_024308867.1:p.Val6554Ala
|
|
XM_024453100.1:c.9515T>C
(TTN)
|
XP_024308868.1:p.Val3172Ala
|
|