ENST00000342992.11:c.98420T>C
(TTN)
|
ENSP00000343764.6:p.Met32807Thr
|
|
ENST00000342175.11:c.79505T>C
(TTN)
|
ENSP00000340554.6:p.Met26502Thr
|
|
ENST00000359218.10:c.79304T>C
(TTN)
|
ENSP00000352154.5:p.Met26435Thr
|
|
ENST00000342175.10:c.79505T>C
(TTN)
|
ENSP00000340554.6:p.Met26502Thr
|
|
ENST00000342992.10:c.98420T>C
(TTN)
|
ENSP00000343764.6:p.Met32807Thr
|
|
ENST00000359218.9:c.79304T>C
(TTN)
|
ENSP00000352154.5:p.Met26435Thr
|
|
ENST00000460472.6:c.78929T>C
(TTN)
|
ENSP00000434586.1:p.Met26310Thr
|
|
ENST00000589042.5:c.106124T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Met35375Thr
|
|
ENST00000591111.5:c.101201T>C
(TTN)
|
ENSP00000465570.1:p.Met33734Thr
|
|
ENST00000615779.4:c.101201T>C
(TTN)
|
ENSP00000483597.1:p.Met33734Thr
|
|
NM_001256850.1:c.101201T>C
(TTN)
|
NP_001243779.1:p.Met33734Thr
|
|
NM_001267550.2:c.106124T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Met35375Thr
|
|
NM_003319.4:c.78929T>C
(TTN)
|
NP_003310.4:p.Met26310Thr
|
|
NM_133378.4:c.98420T>C
(TTN)
|
NP_596869.4:p.Met32807Thr
|
|
NM_133432.3:c.79304T>C
(TTN)
|
NP_597676.3:p.Met26435Thr
|
|
NM_133437.4:c.79505T>C
(TTN)
|
NP_597681.4:p.Met26502Thr
|
|
NR_038271.1:n.446+6855A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5241A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105221T>C
(TTN)
|
XP_011510031.1:p.Met35074Thr
|
|
XM_011511730.1:c.79115T>C
(TTN)
|
XP_011510032.1:p.Met26372Thr
|
|
XM_011511731.1:c.78974T>C
(TTN)
|
XP_011510033.1:p.Met26325Thr
|
|
XM_017004819.1:c.105017T>C
(TTN)
|
XP_016860308.1:p.Met35006Thr
|
|
XM_017004820.1:c.100415T>C
(TTN)
|
XP_016860309.1:p.Met33472Thr
|
|
XM_017004821.1:c.100412T>C
(TTN)
|
XP_016860310.1:p.Met33471Thr
|
|
XM_017004822.1:c.97454T>C
(TTN)
|
XP_016860311.1:p.Met32485Thr
|
|
XM_017004823.1:c.79070T>C
(TTN)
|
XP_016860312.1:p.Met26357Thr
|
|
XM_024453094.1:c.100565T>C
(TTN)
|
XP_024308862.1:p.Met33522Thr
|
|
XM_024453095.1:c.100562T>C
(TTN)
|
XP_024308863.1:p.Met33521Thr
|
|
XM_024453096.1:c.99995T>C
(TTN)
|
XP_024308864.1:p.Met33332Thr
|
|
XM_024453097.1:c.97337T>C
(TTN)
|
XP_024308865.1:p.Met32446Thr
|
|
XM_024453098.1:c.97256T>C
(TTN)
|
XP_024308866.1:p.Met32419Thr
|
|
XM_024453099.1:c.79019T>C
(TTN)
|
XP_024308867.1:p.Met26340Thr
|
|
XM_024453100.1:c.68873T>C
(TTN)
|
XP_024308868.1:p.Met22958Thr
|
|