ENST00000342992.11:c.90393T>C
(TTN)
|
ENSP00000343764.6:p.Leu30131=
|
|
ENST00000342175.11:c.71478T>C
(TTN)
|
ENSP00000340554.6:p.Leu23826=
|
|
ENST00000359218.10:c.71277T>C
(TTN)
|
ENSP00000352154.5:p.Leu23759=
|
|
ENST00000342175.10:c.71478T>C
(TTN)
|
ENSP00000340554.6:p.Leu23826=
|
|
ENST00000342992.10:c.90393T>C
(TTN)
|
ENSP00000343764.6:p.Leu30131=
|
|
ENST00000359218.9:c.71277T>C
(TTN)
|
ENSP00000352154.5:p.Leu23759=
|
|
ENST00000460472.6:c.70902T>C
(TTN)
|
ENSP00000434586.1:p.Leu23634=
|
|
ENST00000589042.5:c.98097T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu32699=
|
|
ENST00000591111.5:c.93174T>C
(TTN)
|
ENSP00000465570.1:p.Leu31058=
|
|
ENST00000615779.4:c.93174T>C
(TTN)
|
ENSP00000483597.1:p.Leu31058=
|
|
NM_001256850.1:c.93174T>C
(TTN)
|
NP_001243779.1:p.Leu31058=
|
|
NM_001267550.2:c.98097T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Leu32699=
|
|
NM_003319.4:c.70902T>C
(TTN)
|
NP_003310.4:p.Leu23634=
|
|
NM_133378.4:c.90393T>C
(TTN)
|
NP_596869.4:p.Leu30131=
|
|
NM_133432.3:c.71277T>C
(TTN)
|
NP_597676.3:p.Leu23759=
|
|
NM_133437.4:c.71478T>C
(TTN)
|
NP_597681.4:p.Leu23826=
|
|
NR_038271.1:n.446+16433A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.1841-38A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.97194T>C
(TTN)
|
XP_011510031.1:p.Leu32398=
|
|
XM_011511730.1:c.71088T>C
(TTN)
|
XP_011510032.1:p.Leu23696=
|
|
XM_011511731.1:c.70947T>C
(TTN)
|
XP_011510033.1:p.Leu23649=
|
|
XM_017004819.1:c.96990T>C
(TTN)
|
XP_016860308.1:p.Leu32330=
|
|
XM_017004820.1:c.92388T>C
(TTN)
|
XP_016860309.1:p.Leu30796=
|
|
XM_017004821.1:c.92385T>C
(TTN)
|
XP_016860310.1:p.Leu30795=
|
|
XM_017004822.1:c.89427T>C
(TTN)
|
XP_016860311.1:p.Leu29809=
|
|
XM_017004823.1:c.71043T>C
(TTN)
|
XP_016860312.1:p.Leu23681=
|
|
XM_024453094.1:c.92538T>C
(TTN)
|
XP_024308862.1:p.Leu30846=
|
|
XM_024453095.1:c.92535T>C
(TTN)
|
XP_024308863.1:p.Leu30845=
|
|
XM_024453096.1:c.91968T>C
(TTN)
|
XP_024308864.1:p.Leu30656=
|
|
XM_024453097.1:c.89310T>C
(TTN)
|
XP_024308865.1:p.Leu29770=
|
|
XM_024453098.1:c.89229T>C
(TTN)
|
XP_024308866.1:p.Leu29743=
|
|
XM_024453099.1:c.70992T>C
(TTN)
|
XP_024308867.1:p.Leu23664=
|
|
XM_024453100.1:c.60846T>C
(TTN)
|
XP_024308868.1:p.Leu20282=
|
|