ENST00000342992.11:c.71036T>C
(TTN)
|
ENSP00000343764.6:p.Phe23679Ser
|
|
ENST00000342175.11:c.52121T>C
(TTN)
|
ENSP00000340554.6:p.Phe17374Ser
|
|
ENST00000359218.10:c.51920T>C
(TTN)
|
ENSP00000352154.5:p.Phe17307Ser
|
|
ENST00000342175.10:c.52121T>C
(TTN)
|
ENSP00000340554.6:p.Phe17374Ser
|
|
ENST00000342992.10:c.71036T>C
(TTN)
|
ENSP00000343764.6:p.Phe23679Ser
|
|
ENST00000359218.9:c.51920T>C
(TTN)
|
ENSP00000352154.5:p.Phe17307Ser
|
|
ENST00000460472.6:c.51545T>C
(TTN)
|
ENSP00000434586.1:p.Phe17182Ser
|
|
ENST00000589042.5:c.78740T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Phe26247Ser
|
|
ENST00000591111.5:c.73817T>C
(TTN)
|
ENSP00000465570.1:p.Phe24606Ser
|
|
ENST00000615779.4:c.73817T>C
(TTN)
|
ENSP00000483597.1:p.Phe24606Ser
|
|
NM_001256850.1:c.73817T>C
(TTN)
|
NP_001243779.1:p.Phe24606Ser
|
|
NM_001267550.2:c.78740T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Phe26247Ser
|
|
NM_003319.4:c.51545T>C
(TTN)
|
NP_003310.4:p.Phe17182Ser
|
|
NM_133378.4:c.71036T>C
(TTN)
|
NP_596869.4:p.Phe23679Ser
|
|
NM_133432.3:c.51920T>C
(TTN)
|
NP_597676.3:p.Phe17307Ser
|
|
NM_133437.4:c.52121T>C
(TTN)
|
NP_597681.4:p.Phe17374Ser
|
|
NR_038271.1:n.447-3908A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-15180A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.77837T>C
(TTN)
|
XP_011510031.1:p.Phe25946Ser
|
|
XM_011511730.1:c.51731T>C
(TTN)
|
XP_011510032.1:p.Phe17244Ser
|
|
XM_011511731.1:c.51590T>C
(TTN)
|
XP_011510033.1:p.Phe17197Ser
|
|
XM_017004819.1:c.77633T>C
(TTN)
|
XP_016860308.1:p.Phe25878Ser
|
|
XM_017004820.1:c.73031T>C
(TTN)
|
XP_016860309.1:p.Phe24344Ser
|
|
XM_017004821.1:c.73028T>C
(TTN)
|
XP_016860310.1:p.Phe24343Ser
|
|
XM_017004822.1:c.70070T>C
(TTN)
|
XP_016860311.1:p.Phe23357Ser
|
|
XM_017004823.1:c.51686T>C
(TTN)
|
XP_016860312.1:p.Phe17229Ser
|
|
XM_024453094.1:c.73181T>C
(TTN)
|
XP_024308862.1:p.Phe24394Ser
|
|
XM_024453095.1:c.73178T>C
(TTN)
|
XP_024308863.1:p.Phe24393Ser
|
|
XM_024453096.1:c.72611T>C
(TTN)
|
XP_024308864.1:p.Phe24204Ser
|
|
XM_024453097.1:c.69953T>C
(TTN)
|
XP_024308865.1:p.Phe23318Ser
|
|
XM_024453098.1:c.69872T>C
(TTN)
|
XP_024308866.1:p.Phe23291Ser
|
|
XM_024453099.1:c.51635T>C
(TTN)
|
XP_024308867.1:p.Phe17212Ser
|
|
XM_024453100.1:c.41489T>C
(TTN)
|
XP_024308868.1:p.Phe13830Ser
|
|