ENST00000342992.11:c.96818G>C
(TTN)
|
ENSP00000343764.6:p.Arg32273Pro
|
|
ENST00000342175.11:c.77903G>C
(TTN)
|
ENSP00000340554.6:p.Arg25968Pro
|
|
ENST00000359218.10:c.77702G>C
(TTN)
|
ENSP00000352154.5:p.Arg25901Pro
|
|
ENST00000342175.10:c.77903G>C
(TTN)
|
ENSP00000340554.6:p.Arg25968Pro
|
|
ENST00000342992.10:c.96818G>C
(TTN)
|
ENSP00000343764.6:p.Arg32273Pro
|
|
ENST00000359218.9:c.77702G>C
(TTN)
|
ENSP00000352154.5:p.Arg25901Pro
|
|
ENST00000460472.6:c.77327G>C
(TTN)
|
ENSP00000434586.1:p.Arg25776Pro
|
|
ENST00000589042.5:c.104522G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg34841Pro
|
|
ENST00000591111.5:c.99599G>C
(TTN)
|
ENSP00000465570.1:p.Arg33200Pro
|
|
ENST00000615779.4:c.99599G>C
(TTN)
|
ENSP00000483597.1:p.Arg33200Pro
|
|
NM_001256850.1:c.99599G>C
(TTN)
|
NP_001243779.1:p.Arg33200Pro
|
|
NM_001267550.2:c.104522G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Arg34841Pro
|
|
NM_003319.4:c.77327G>C
(TTN)
|
NP_003310.4:p.Arg25776Pro
|
|
NM_133378.4:c.96818G>C
(TTN)
|
NP_596869.4:p.Arg32273Pro
|
|
NM_133432.3:c.77702G>C
(TTN)
|
NP_597676.3:p.Arg25901Pro
|
|
NM_133437.4:c.77903G>C
(TTN)
|
NP_597681.4:p.Arg25968Pro
|
|
NR_038271.1:n.446+8457C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3639C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.103619G>C
(TTN)
|
XP_011510031.1:p.Arg34540Pro
|
|
XM_011511730.1:c.77513G>C
(TTN)
|
XP_011510032.1:p.Arg25838Pro
|
|
XM_011511731.1:c.77372G>C
(TTN)
|
XP_011510033.1:p.Arg25791Pro
|
|
XM_017004819.1:c.103415G>C
(TTN)
|
XP_016860308.1:p.Arg34472Pro
|
|
XM_017004820.1:c.98813G>C
(TTN)
|
XP_016860309.1:p.Arg32938Pro
|
|
XM_017004821.1:c.98810G>C
(TTN)
|
XP_016860310.1:p.Arg32937Pro
|
|
XM_017004822.1:c.95852G>C
(TTN)
|
XP_016860311.1:p.Arg31951Pro
|
|
XM_017004823.1:c.77468G>C
(TTN)
|
XP_016860312.1:p.Arg25823Pro
|
|
XM_024453094.1:c.98963G>C
(TTN)
|
XP_024308862.1:p.Arg32988Pro
|
|
XM_024453095.1:c.98960G>C
(TTN)
|
XP_024308863.1:p.Arg32987Pro
|
|
XM_024453096.1:c.98393G>C
(TTN)
|
XP_024308864.1:p.Arg32798Pro
|
|
XM_024453097.1:c.95735G>C
(TTN)
|
XP_024308865.1:p.Arg31912Pro
|
|
XM_024453098.1:c.95654G>C
(TTN)
|
XP_024308866.1:p.Arg31885Pro
|
|
XM_024453099.1:c.77417G>C
(TTN)
|
XP_024308867.1:p.Arg25806Pro
|
|
XM_024453100.1:c.67271G>C
(TTN)
|
XP_024308868.1:p.Arg22424Pro
|
|