ENST00000342992.11:c.98720T>C
(TTN)
|
ENSP00000343764.6:p.Phe32907Ser
|
|
ENST00000342175.11:c.79805T>C
(TTN)
|
ENSP00000340554.6:p.Phe26602Ser
|
|
ENST00000359218.10:c.79604T>C
(TTN)
|
ENSP00000352154.5:p.Phe26535Ser
|
|
ENST00000342175.10:c.79805T>C
(TTN)
|
ENSP00000340554.6:p.Phe26602Ser
|
|
ENST00000342992.10:c.98720T>C
(TTN)
|
ENSP00000343764.6:p.Phe32907Ser
|
|
ENST00000359218.9:c.79604T>C
(TTN)
|
ENSP00000352154.5:p.Phe26535Ser
|
|
ENST00000460472.6:c.79229T>C
(TTN)
|
ENSP00000434586.1:p.Phe26410Ser
|
|
ENST00000589042.5:c.106424T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Phe35475Ser
|
|
ENST00000591111.5:c.101501T>C
(TTN)
|
ENSP00000465570.1:p.Phe33834Ser
|
|
ENST00000615779.4:c.101501T>C
(TTN)
|
ENSP00000483597.1:p.Phe33834Ser
|
|
NM_001256850.1:c.101501T>C
(TTN)
|
NP_001243779.1:p.Phe33834Ser
|
|
NM_001267550.2:c.106424T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Phe35475Ser
|
|
NM_003319.4:c.79229T>C
(TTN)
|
NP_003310.4:p.Phe26410Ser
|
|
NM_133378.4:c.98720T>C
(TTN)
|
NP_596869.4:p.Phe32907Ser
|
|
NM_133432.3:c.79604T>C
(TTN)
|
NP_597676.3:p.Phe26535Ser
|
|
NM_133437.4:c.79805T>C
(TTN)
|
NP_597681.4:p.Phe26602Ser
|
|
NR_038271.1:n.446+6431A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5665A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105521T>C
(TTN)
|
XP_011510031.1:p.Phe35174Ser
|
|
XM_011511730.1:c.79415T>C
(TTN)
|
XP_011510032.1:p.Phe26472Ser
|
|
XM_011511731.1:c.79274T>C
(TTN)
|
XP_011510033.1:p.Phe26425Ser
|
|
XM_017004819.1:c.105317T>C
(TTN)
|
XP_016860308.1:p.Phe35106Ser
|
|
XM_017004820.1:c.100715T>C
(TTN)
|
XP_016860309.1:p.Phe33572Ser
|
|
XM_017004821.1:c.100712T>C
(TTN)
|
XP_016860310.1:p.Phe33571Ser
|
|
XM_017004822.1:c.97754T>C
(TTN)
|
XP_016860311.1:p.Phe32585Ser
|
|
XM_017004823.1:c.79370T>C
(TTN)
|
XP_016860312.1:p.Phe26457Ser
|
|
XM_024453094.1:c.100865T>C
(TTN)
|
XP_024308862.1:p.Phe33622Ser
|
|
XM_024453095.1:c.100862T>C
(TTN)
|
XP_024308863.1:p.Phe33621Ser
|
|
XM_024453096.1:c.100295T>C
(TTN)
|
XP_024308864.1:p.Phe33432Ser
|
|
XM_024453097.1:c.97637T>C
(TTN)
|
XP_024308865.1:p.Phe32546Ser
|
|
XM_024453098.1:c.97556T>C
(TTN)
|
XP_024308866.1:p.Phe32519Ser
|
|
XM_024453099.1:c.79319T>C
(TTN)
|
XP_024308867.1:p.Phe26440Ser
|
|
XM_024453100.1:c.69173T>C
(TTN)
|
XP_024308868.1:p.Phe23058Ser
|
|