ENST00000342992.11:c.39057G>T
(TTN)
|
ENSP00000343764.6:p.Met13019Ile
|
|
ENST00000342175.11:c.20142G>T
(TTN)
|
ENSP00000340554.6:p.Met6714Ile
|
|
ENST00000359218.10:c.19941G>T
(TTN)
|
ENSP00000352154.5:p.Met6647Ile
|
|
ENST00000342175.10:c.20142G>T
(TTN)
|
ENSP00000340554.6:p.Met6714Ile
|
|
ENST00000342992.10:c.39057G>T
(TTN)
|
ENSP00000343764.6:p.Met13019Ile
|
|
ENST00000359218.9:c.19941G>T
(TTN)
|
ENSP00000352154.5:p.Met6647Ile
|
|
ENST00000460472.6:c.19566G>T
(TTN)
|
ENSP00000434586.1:p.Met6522Ile
|
|
ENST00000589042.5:c.46761G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Met15587Ile
|
|
ENST00000591111.5:c.41838G>T
(TTN)
|
ENSP00000465570.1:p.Met13946Ile
|
|
ENST00000615779.4:c.41838G>T
(TTN)
|
ENSP00000483597.1:p.Met13946Ile
|
|
NM_001256850.1:c.41838G>T
(TTN)
|
NP_001243779.1:p.Met13946Ile
|
|
NM_001267550.2:c.46761G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Met15587Ile
|
|
NM_003319.4:c.19566G>T
(TTN)
|
NP_003310.4:p.Met6522Ile
|
|
NM_133378.4:c.39057G>T
(TTN)
|
NP_596869.4:p.Met13019Ile
|
|
NM_133432.3:c.19941G>T
(TTN)
|
NP_597676.3:p.Met6647Ile
|
|
NM_133437.4:c.20142G>T
(TTN)
|
NP_597681.4:p.Met6714Ile
|
|
NR_038271.1:n.1605-964C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.45858G>T
(TTN)
|
XP_011510031.1:p.Met15286Ile
|
|
XM_011511730.1:c.19752G>T
(TTN)
|
XP_011510032.1:p.Met6584Ile
|
|
XM_011511731.1:c.19611G>T
(TTN)
|
XP_011510033.1:p.Met6537Ile
|
|
XM_017004819.1:c.45654G>T
(TTN)
|
XP_016860308.1:p.Met15218Ile
|
|
XM_017004820.1:c.41052G>T
(TTN)
|
XP_016860309.1:p.Met13684Ile
|
|
XM_017004821.1:c.41049G>T
(TTN)
|
XP_016860310.1:p.Met13683Ile
|
|
XM_017004822.1:c.38091G>T
(TTN)
|
XP_016860311.1:p.Met12697Ile
|
|
XM_017004823.1:c.19707G>T
(TTN)
|
XP_016860312.1:p.Met6569Ile
|
|
XM_024453094.1:c.41202G>T
(TTN)
|
XP_024308862.1:p.Met13734Ile
|
|
XM_024453095.1:c.41199G>T
(TTN)
|
XP_024308863.1:p.Met13733Ile
|
|
XM_024453096.1:c.40632G>T
(TTN)
|
XP_024308864.1:p.Met13544Ile
|
|
XM_024453097.1:c.37974G>T
(TTN)
|
XP_024308865.1:p.Met12658Ile
|
|
XM_024453098.1:c.37893G>T
(TTN)
|
XP_024308866.1:p.Met12631Ile
|
|
XM_024453099.1:c.19656G>T
(TTN)
|
XP_024308867.1:p.Met6552Ile
|
|
XM_024453100.1:c.9510G>T
(TTN)
|
XP_024308868.1:p.Met3170Ile
|
|